Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155812271C= , CM000669.2:g.155812271C= | GRCh38 |
| NC_000007.13:g.155604965C= , CM000669.1:g.155604965C= | GRCh37 |
| NC_000007.12:g.155297726C= | NCBI36 |
| NG_007504.2:g.5003G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297261.7:c.-149G= MANE Select | ENSP00000297261.2:n.-149G= | |
| ENST00000297261.6:c.-149G= | ENSP00000297261.2:n.-149G= | |
| NM_000193.2:c.-149G= | NP_000184.1:n.-149G= | |
| NM_000193.3:c.-149G= | NP_000184.1:n.-149G= | |
| NM_000193.4:c.-149G= MANE Select | NP_000184.1:n.-149G= |