Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6587172C>T , CM000671.2:g.6587172C>T | GRCh38 |
| NC_000009.11:g.6587172C>T , CM000671.1:g.6587172C>T | GRCh37 |
| NC_000009.10:g.6577172C>T | NCBI36 |
| NG_016397.1:g.63521G>A , LRG_643:g.63521G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000170.3:c.1819G>A MANE Select | NP_000161.2:p.Gly607Ser |
| ENST00000321612.8:c.1819G>A MANE Select | ENSP00000370737.4:p.Gly607Ser |
| NM_000170.2:c.1819G>A , LRG_643t1:c.1819G>A | NP_000161.2:p.Gly607Ser |
| ENST00000321612.6:c.1819G>A | ENSP00000370737.3:p.Gly607Ser |
| ENST00000639364.1:n.1519G>A | |
| ENST00000639443.1:n.1387G>A | |
| ENST00000639954.1:n.1527G>A | |
| ENST00000640592.1:n.1702G>A |