Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255749G= , CM000671.2:g.133255749G= | GRCh38 |
| NC_000009.11:g.136131136G= , CM000671.1:g.136131136G= | GRCh37 |
| NC_000009.10:g.135120957G= | NCBI36 |
| NG_006669.1:g.21919C= | |
| NG_006669.2:g.24467C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1011C= | ||
| ENST00000647353.1:n.54-4597C= | ||
| ENST00000679909.1:c.28+19413C= | ENSP00000506089.1:n.28+19413C= | |
| ENST00000453660.3:n.993C= | ||
| ENST00000538324.2:c.979C= | ENSP00000483018.1:p.Gln327= | |
| ENST00000611156.4:c.979C= | ENSP00000483265.1:p.Gln327= | |
| NM_020469.2:c.982C= | NP_065202.2:p.Gln328= | |
| NM_020469.3:c.982C= | NP_065202.2:p.Gln328= |