Linked Data
dbSNP Id:
rs890171780
gnomAD v2:
1-214830930-A-G
gnomAD v3:
1-214657587-A-G
gnomAD v4:
1-214657587-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.214657587A>G , CM000663.2:g.214657587A>G | GRCh38 |
| NC_000001.10:g.214830930A>G , CM000663.1:g.214830930A>G | GRCh37 |
| NC_000001.9:g.212897553A>G | NCBI36 |
| NG_046787.1:g.59409A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706765.1:c.8785+178A>G | ENSP00000516538.1:n.8785+178A>G | |
| ENST00000706766.1:n.1061+178A>G | ||
| ENST00000366955.8:c.8962+178A>G MANE Select | ENSP00000355922.3:n.8962+178A>G | |
| ENST00000366955.7:c.8962+178A>G | ENSP00000355922.3:n.8962+178A>G | |
| NM_016343.3:c.8962+178A>G | NP_057427.3:n.8962+178A>G | |
| XM_011509082.1:c.8785+178A>G | XP_011507384.1:n.8785+178A>G | |
| XM_011509083.1:c.7897+178A>G | XP_011507385.1:n.7897+178A>G | |
| XM_011509082.3:c.8785+178A>G | XP_011507384.1:n.8785+178A>G | |
| XM_017000086.2:c.8962+178A>G | XP_016855575.1:n.8962+178A>G | |
| NM_016343.4:c.8962+178A>G MANE Select | NP_057427.3:n.8962+178A>G |