Linked Data
ClinVar Variation Id:
282408
dbSNP Id:
rs762258343
ExAC:
2:71896838 T / C
gnomAD v2:
2-71896838-T-C
gnomAD v4:
2-71669708-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71669708T>C , CM000664.2:g.71669708T>C | GRCh38 |
| NC_000002.11:g.71896838T>C , CM000664.1:g.71896838T>C | GRCh37 |
| NC_000002.10:g.71750346T>C | NCBI36 |
| NG_008694.1:g.221086T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.3160T>C | ENSP00000513536.1:p.Tyr1054His | |
| ENST00000698058.1:c.2377T>C | ENSP00000513537.1:p.Tyr793His | |
| ENST00000698059.1:c.2485T>C | ENSP00000513538.1:p.Tyr829His | |
| ENST00000258104.8:c.5629T>C MANE Plus Clinical | ENSP00000258104.3:p.Tyr1877His | |
| ENST00000410020.8:c.5746T>C MANE Select | ENSP00000386881.3:p.Tyr1916His | |
| ENST00000258104.7:c.5629T>C | ENSP00000258104.3:p.Tyr1877His | |
| ENST00000394120.6:c.5632T>C | ENSP00000377678.2:p.Tyr1878His | |
| ENST00000409366.5:c.5695T>C | ENSP00000386512.1:p.Tyr1899His | |
| ENST00000409582.7:c.5743T>C | ENSP00000386547.3:p.Tyr1915His | |
| ENST00000409651.5:c.5725T>C | ENSP00000386683.1:p.Tyr1909His | |
| ENST00000409744.5:c.5653T>C | ENSP00000386285.1:p.Tyr1885His | |
| ENST00000409762.5:c.5680T>C | ENSP00000387137.1:p.Tyr1894His | |
| ENST00000410020.7:c.5746T>C | ENSP00000386881.3:p.Tyr1916His | |
| ENST00000410041.1:c.5683T>C | ENSP00000386617.1:p.Tyr1895His | |
| ENST00000413539.6:c.5722T>C | ENSP00000407046.2:p.Tyr1908His | |
| ENST00000429174.6:c.5692T>C | ENSP00000398305.2:p.Tyr1898His | |
| ENST00000479049.6:n.2514T>C | ||
| NM_001130455.1:c.5632T>C | NP_001123927.1:p.Tyr1878His | |
| NM_001130976.1:c.5587T>C | NP_001124448.1:p.Tyr1863His | |
| NM_001130977.1:c.5650T>C | NP_001124449.1:p.Tyr1884His | |
| NM_001130978.1:c.5692T>C | NP_001124450.1:p.Tyr1898His | |
| NM_001130979.1:c.5722T>C | NP_001124451.1:p.Tyr1908His | |
| NM_001130980.1:c.5680T>C | NP_001124452.1:p.Tyr1894His | |
| NM_001130981.1:c.5743T>C | NP_001124453.1:p.Tyr1915His | |
| NM_001130982.1:c.5725T>C | NP_001124454.1:p.Tyr1909His | |
| NM_001130983.1:c.5695T>C | NP_001124455.1:p.Tyr1899His | |
| NM_001130984.1:c.5653T>C | NP_001124456.1:p.Tyr1885His | |
| NM_001130985.1:c.5683T>C | NP_001124457.1:p.Tyr1895His | |
| NM_001130986.1:c.5590T>C | NP_001124458.1:p.Tyr1864His | |
| NM_001130987.1:c.5746T>C | NP_001124459.1:p.Tyr1916His | |
| NM_003494.3:c.5629T>C | NP_003485.1:p.Tyr1877His | |
| XM_005264584.3:c.5788T>C | XP_005264641.1:p.Tyr1930His | |
| XM_005264585.3:c.5785T>C | XP_005264642.1:p.Tyr1929His | |
| XM_005264584.4:c.5788T>C | XP_005264641.1:p.Tyr1930His | |
| XM_005264585.5:c.5785T>C | XP_005264642.1:p.Tyr1929His | |
| NM_001130987.2:c.5746T>C MANE Select | NP_001124459.1:p.Tyr1916His | |
| NM_001130455.2:c.5632T>C | NP_001123927.1:p.Tyr1878His | |
| NM_001130976.2:c.5587T>C | NP_001124448.1:p.Tyr1863His | |
| NM_001130977.2:c.5650T>C | NP_001124449.1:p.Tyr1884His | |
| NM_001130978.2:c.5692T>C | NP_001124450.1:p.Tyr1898His | |
| NM_001130979.2:c.5722T>C | NP_001124451.1:p.Tyr1908His | |
| NM_001130980.2:c.5680T>C | NP_001124452.1:p.Tyr1894His | |
| NM_001130981.2:c.5743T>C | NP_001124453.1:p.Tyr1915His | |
| NM_001130982.2:c.5725T>C | NP_001124454.1:p.Tyr1909His | |
| NM_001130983.2:c.5695T>C | NP_001124455.1:p.Tyr1899His | |
| NM_001130984.2:c.5653T>C | NP_001124456.1:p.Tyr1885His | |
| NM_001130985.2:c.5683T>C | NP_001124457.1:p.Tyr1895His | |
| NM_001130986.2:c.5590T>C | NP_001124458.1:p.Tyr1864His | |
| NM_003494.4:c.5629T>C MANE Plus Clinical | NP_003485.1:p.Tyr1877His |