Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15191774T= , CM000681.2:g.15191774T= | GRCh38 |
| NC_000019.9:g.15302585T= , CM000681.1:g.15302585T= | GRCh37 |
| NC_000019.8:g.15163585T= | NCBI36 |
| NG_009819.1:g.14208A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.773A= MANE Select | ENSP00000263388.1:p.Tyr258= | |
| ENST00000263388.6:c.773A= | ENSP00000263388.1:p.Tyr258= | |
| ENST00000601011.1:c.770A= | ENSP00000473138.1:p.Tyr257= | |
| NM_000435.2:c.773A= | NP_000426.2:p.Tyr258= | |
| XM_005259924.3:c.773A= | XP_005259981.1:p.Tyr258= | |
| XM_005259924.4:c.773A= | XP_005259981.1:p.Tyr258= | |
| NM_000435.3:c.773A= MANE Select | NP_000426.2:p.Tyr258= |