UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
dbSNP Id:
rs2125377422
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12599709A>G , CM000665.2:g.12599709A>G | GRCh38 |
| NC_000003.11:g.12641208A>G , CM000665.1:g.12641208A>G | GRCh37 |
| NC_000003.10:g.12616208A>G | NCBI36 |
| NG_007467.1:g.69471T>C , LRG_413:g.69471T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000423275.6:c.*755T>C | ENSP00000401088.1:n.*755T>C | |
| ENST00000432427.3:c.410T>C | ||
| ENST00000465826.6:n.681T>C | ||
| ENST00000491290.2:n.1467T>C | ||
| ENST00000684903.1:c.*767T>C | ENSP00000508612.1:n.*767T>C | |
| ENST00000685348.1:c.*767T>C | ENSP00000510285.1:n.*767T>C | |
| ENST00000685437.1:c.991T>C | ENSP00000508794.1:p.Tyr331His | |
| ENST00000685653.1:c.1090T>C | ENSP00000509968.1:p.Tyr364His | |
| ENST00000685738.1:c.1090T>C | ENSP00000510156.1:p.Tyr364His | |
| ENST00000686409.1:n.2141T>C | ||
| ENST00000686455.1:n.1453T>C | ||
| ENST00000686479.1:n.1461T>C | ||
| ENST00000686762.1:c.1090T>C | ENSP00000509767.1:p.Tyr364His | |
| ENST00000687257.1:n.1326T>C | ||
| ENST00000687326.1:c.1090T>C | ENSP00000509665.1:p.Tyr364His | |
| ENST00000687486.1:c.282T>C | ||
| ENST00000687505.1:n.1208T>C | ||
| ENST00000687923.1:c.991T>C | ENSP00000510255.1:p.Tyr331His | |
| ENST00000687940.1:n.1467T>C | ||
| ENST00000688269.1:n.1686T>C | ||
| ENST00000688326.1:c.410T>C | ||
| ENST00000688444.1:n.1416T>C | ||
| ENST00000688543.1:c.991T>C | ENSP00000509612.1:p.Tyr331His | |
| ENST00000688625.1:c.*668T>C | ENSP00000509522.1:n.*668T>C | |
| ENST00000688803.1:n.1321T>C | ||
| ENST00000688914.1:n.76T>C | ||
| ENST00000689097.1:c.*767T>C | ENSP00000509756.1:n.*767T>C | |
| ENST00000689389.1:c.1090T>C | ENSP00000510213.1:p.Tyr364His | |
| ENST00000689418.1:c.*767T>C | ENSP00000509467.1:n.*767T>C | |
| ENST00000689481.1:c.*767T>C | ENSP00000510248.1:n.*767T>C | |
| ENST00000689540.1:n.1240T>C | ||
| ENST00000689876.1:c.1090T>C | ENSP00000508535.1:p.Tyr364His | |
| ENST00000689914.1:c.1090T>C | ENSP00000509847.1:p.Tyr364His | |
| ENST00000690397.1:c.979T>C | ENSP00000508730.1:p.Tyr327His | |
| ENST00000690460.1:c.1078T>C | ENSP00000509106.1:p.Tyr360His | |
| ENST00000690625.1:n.1393T>C | ||
| ENST00000691268.1:c.517T>C | ||
| ENST00000691396.1:c.*883T>C | ENSP00000510712.1:n.*883T>C | |
| ENST00000691724.1:c.*47T>C | ENSP00000509255.1:n.*47T>C | |
| ENST00000691779.1:c.*668T>C | ENSP00000508592.1:n.*668T>C | |
| ENST00000691899.1:c.1090T>C | ENSP00000508763.1:p.Tyr364His | |
| ENST00000692069.1:n.1656T>C | ||
| ENST00000692093.1:c.991T>C | ENSP00000509669.1:p.Tyr331His | |
| ENST00000692311.1:n.1914T>C | ||
| ENST00000692558.1:n.1455T>C | ||
| ENST00000692773.1:c.*827T>C | ENSP00000509055.1:n.*827T>C | |
| ENST00000692830.1:c.*835T>C | ENSP00000509461.1:n.*835T>C | |
| ENST00000693069.1:c.991T>C | ENSP00000510072.1:p.Tyr331His | |
| ENST00000693312.1:c.865T>C | ENSP00000508686.1:p.Tyr289His | |
| ENST00000693664.1:c.1090T>C | ENSP00000509614.1:p.Tyr364His | |
| ENST00000693705.1:c.*767T>C | ENSP00000510697.1:n.*767T>C | |
| ENST00000251849.9:c.1090T>C MANE Select | ENSP00000251849.4:p.Tyr364His | |
| ENST00000442415.7:c.1150T>C | ENSP00000401888.2:p.Tyr384His | |
| ENST00000251849.8:c.1090T>C | ENSP00000251849.4:p.Tyr364His | |
| ENST00000423275.5:c.*767T>C | ENSP00000401088.1:n.*767T>C | |
| ENST00000432427.2:c.727T>C | ENSP00000398591.2:p.Tyr243His | |
| ENST00000442415.6:c.1150T>C | ENSP00000401888.2:p.Tyr384His | |
| ENST00000460610.1:n.47T>C | ||
| ENST00000465826.5:n.334T>C | ||
| NM_002880.3:c.1090T>C , LRG_413t1:c.1090T>C | NP_002871.1:p.Tyr364His | |
| XM_005265355.1:c.1090T>C | XP_005265412.1:p.Tyr364His | |
| XM_005265357.1:c.991T>C | XP_005265414.1:p.Tyr331His | |
| XM_005265358.3:c.847T>C | XP_005265415.1:p.Tyr283His | |
| XM_005265359.3:c.748T>C | XP_005265416.1:p.Tyr250His | |
| XM_005265360.1:c.1090T>C | XP_005265417.1:p.Tyr364His | |
| XM_011533974.1:c.1090T>C | XP_011532276.1:p.Tyr364His | |
| XM_011533975.1:c.847T>C | XP_011532277.1:p.Tyr283His | |
| NM_001354689.1:c.1150T>C | NP_001341618.1:p.Tyr384His | |
| NM_001354690.1:c.1090T>C | NP_001341619.1:p.Tyr364His | |
| NM_001354691.1:c.847T>C | NP_001341620.1:p.Tyr283His | |
| NM_001354692.1:c.847T>C | NP_001341621.1:p.Tyr283His | |
| NM_001354693.1:c.991T>C | NP_001341622.1:p.Tyr331His | |
| NM_001354694.1:c.907T>C | NP_001341623.1:p.Tyr303His | |
| NM_001354695.1:c.748T>C | NP_001341624.1:p.Tyr250His | |
| NR_148940.1:n.1505T>C | ||
| NR_148941.1:n.1505T>C | ||
| NR_148942.1:n.1503T>C | ||
| XM_011533974.3:c.1090T>C | XP_011532276.1:p.Tyr364His | |
| XM_017006966.1:c.991T>C | XP_016862455.1:p.Tyr331His | |
| XR_001740227.1:n.1322T>C | ||
| NM_001354689.3:c.1150T>C | NP_001341618.1:p.Tyr384His | |
| NM_001354690.2:c.1090T>C | NP_001341619.1:p.Tyr364His | |
| NM_001354691.2:c.847T>C | NP_001341620.1:p.Tyr283His | |
| NM_001354692.2:c.847T>C | NP_001341621.1:p.Tyr283His | |
| NM_001354693.2:c.991T>C | NP_001341622.1:p.Tyr331His | |
| NM_001354694.2:c.907T>C | NP_001341623.1:p.Tyr303His | |
| NM_001354695.2:c.748T>C | NP_001341624.1:p.Tyr250His | |
| NR_148940.2:n.1421T>C | ||
| NR_148941.2:n.1421T>C | ||
| NR_148942.2:n.1419T>C | ||
| NM_001354690.3:c.1090T>C | NP_001341619.1:p.Tyr364His | |
| NM_001354691.3:c.847T>C | NP_001341620.1:p.Tyr283His | |
| NM_001354692.3:c.847T>C | NP_001341621.1:p.Tyr283His | |
| NM_001354693.3:c.991T>C | NP_001341622.1:p.Tyr331His | |
| NM_001354694.3:c.907T>C | NP_001341623.1:p.Tyr303His | |
| NM_001354695.3:c.748T>C | NP_001341624.1:p.Tyr250His | |
| NM_002880.4:c.1090T>C MANE Select | NP_002871.1:p.Tyr364His | |
| NR_148940.3:n.1421T>C | ||
| NR_148941.3:n.1421T>C | ||
| NR_148942.3:n.1419T>C |