Linked Data
dbSNP Id:
rs11725509
gnomAD v2:
4-149311728-A-C
gnomAD v3:
4-148390576-A-C
gnomAD v4:
4-148390576-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.148390576A>C , CM000666.2:g.148390576A>C | GRCh38 |
| NC_000004.11:g.149311728A>C , CM000666.1:g.149311728A>C | GRCh37 |
| NC_000004.10:g.149531178A>C | NCBI36 |
| NG_013350.1:g.56945T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000358102.8:c.1757+44528T>G MANE Select | ENSP00000350815.3:n.1757+44528T>G | |
| ENST00000342437.8:c.1757+44528T>G | ENSP00000343907.4:n.1757+44528T>G | |
| ENST00000344721.8:c.1757+44528T>G | ENSP00000341390.4:n.1757+44528T>G | |
| ENST00000358102.7:c.1757+44528T>G | ENSP00000350815.3:n.1757+44528T>G | |
| ENST00000511528.1:c.1757+44528T>G | ENSP00000421481.1:n.1757+44528T>G | |
| ENST00000512865.5:c.1757+44528T>G | ENSP00000423510.1:n.1757+44528T>G | |
| ENST00000625323.2:c.1757+44528T>G | ENSP00000486719.1:n.1757+44528T>G | |
| NM_000901.4:c.1757+44528T>G | NP_000892.2:n.1757+44528T>G | |
| NM_001166104.1:c.1757+44528T>G | NP_001159576.1:n.1757+44528T>G | |
| XM_011531975.1:c.1757+44528T>G | XP_011530277.1:n.1757+44528T>G | |
| XM_011531976.1:c.1757+44528T>G | XP_011530278.1:n.1757+44528T>G | |
| XM_011531977.1:c.1757+44528T>G | XP_011530279.1:n.1757+44528T>G | |
| XM_011531978.1:c.1757+44528T>G | XP_011530280.1:n.1757+44528T>G | |
| NM_001354819.1:c.1757+44528T>G | NP_001341748.1:n.1757+44528T>G | |
| NR_148974.1:n.2120+44528T>G | ||
| XM_011531978.2:c.1757+44528T>G | XP_011530280.1:n.1757+44528T>G | |
| NM_000901.5:c.1757+44528T>G MANE Select | NP_000892.2:n.1757+44528T>G | |
| NM_001166104.2:c.1757+44528T>G | NP_001159576.1:n.1757+44528T>G | |
| NR_148974.2:n.2014+44528T>G |