dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148203924C>T , CM000669.2:g.148203924C>T | GRCh38 |
| NC_000007.13:g.147901016C>T , CM000669.1:g.147901016C>T | GRCh37 |
| NC_000007.12:g.147531949C>T | NCBI36 |
| NG_007092.2:g.2092564C>T | |
| NG_007092.3:g.2092924C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.3011-13364C>T MANE Select | ENSP00000354778.3:n.3011-13364C>T | |
| ENST00000636870.1:n.2873-13364C>T | ||
| ENST00000637020.1:n.829-13364C>T | ||
| ENST00000361727.7:c.3011-13364C>T | ENSP00000354778.3:n.3011-13364C>T | |
| ENST00000627772.2:n.1184-13364C>T | ||
| ENST00000628930.2:c.188-13364C>T | ENSP00000487516.1:n.188-13364C>T | |
| NM_014141.5:c.3011-13364C>T | NP_054860.1:n.3011-13364C>T | |
| XM_006715919.1:c.1499-13364C>T | XP_006715982.1:n.1499-13364C>T | |
| NM_014141.6:c.3011-13364C>T MANE Select | NP_054860.1:n.3011-13364C>T |