Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129813794G>T , CM000671.2:g.129813794G>T | GRCh38 |
| NC_000009.11:g.132576073G>T , CM000671.1:g.132576073G>T | GRCh37 |
| NC_000009.10:g.131615894G>T | NCBI36 |
| NG_008049.1:g.15369C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.*178C>A MANE Select | ENSP00000345719.4:n.*178C>A | |
| ENST00000651202.1:c.*445C>A | ENSP00000498222.1:n.*445C>A | |
| ENST00000351698.4:c.*178C>A | ENSP00000345719.4:n.*178C>A | |
| ENST00000474192.1:n.761C>A | ||
| NM_000113.2:c.*178C>A | NP_000104.1:n.*178C>A | |
| XR_929731.3:n.1372C>A | ||
| NM_000113.3:c.*178C>A MANE Select | NP_000104.1:n.*178C>A |