Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136674805C>A , CM000671.2:g.136674805C>A | GRCh38 |
| NC_000009.11:g.139569257C>A , CM000671.1:g.139569257C>A | GRCh37 |
| NC_000009.10:g.138689078C>A | NCBI36 |
| NG_008090.1:g.17655G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.591G>T MANE Select | ENSP00000360761.2:p.Val197= | |
| ENST00000371694.7:c.495G>T | ENSP00000360759.3:p.Val165= | |
| ENST00000371696.6:c.591G>T | ENSP00000360761.2:p.Val197= | |
| ENST00000472820.1:n.519G>T | ||
| ENST00000538402.1:c.591G>T | ENSP00000438919.1:p.Val197= | |
| NM_001012727.1:c.495G>T | NP_001012745.1:p.Val165= | |
| NM_006412.3:c.591G>T | NP_006403.2:p.Val197= | |
| NM_006412.4:c.591G>T MANE Select | NP_006403.2:p.Val197= | |
| NM_001012727.2:c.495G>T | NP_001012745.1:p.Val165= |