Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8087385C>A , CM000679.2:g.8087385C>A | GRCh38 |
| NC_000017.10:g.7990703C>A , CM000679.1:g.7990703C>A | GRCh37 |
| NC_000017.9:g.7931428C>A | NCBI36 |
| NG_007099.1:g.5319G>T | |
| NG_007099.2:g.5332G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.58G>T MANE Select | NP_001130.1:p.Asp20Tyr |
| ENST00000647874.1:c.58G>T MANE Select | ENSP00000497784.1:p.Asp20Tyr |
| NM_001139.2:c.58G>T | NP_001130.1:p.Asp20Tyr |
| ENST00000319144.4:c.58G>T | ENSP00000315167.4:p.Asp20Tyr |