Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.129203437G>A , CM000669.2:g.129203437G>A | GRCh38 |
| NC_000007.13:g.128843278G>A , CM000669.1:g.128843278G>A | GRCh37 |
| NC_000007.12:g.128630514G>A | NCBI36 |
| NG_023340.1:g.19566G>A | |
| NG_023340.2:g.19566G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005631.5:c.385G>A MANE Select | NP_005622.1:p.Val129Ile |
| ENST00000249373.8:c.385G>A MANE Select | ENSP00000249373.3:p.Val129Ile |
| NM_005631.4:c.385G>A | NP_005622.1:p.Val129Ile |
| ENST00000249373.7:c.385G>A | ENSP00000249373.3:p.Val129Ile |
| ENST00000655644.1:c.*249G>A | ENSP00000499377.1:n.*249G>A |
| XM_011516522.1:c.-6G>A | XP_011514824.1:n.-6G>A |
| XM_024446891.1:c.-6G>A | XP_024302659.1:n.-6G>A |