Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.170289628A>C , CM000668.2:g.170289628A>C | GRCh38 |
| NC_000006.11:g.170598716A>C , CM000668.1:g.170598716A>C | GRCh37 |
| NC_000006.10:g.170440641A>C | NCBI36 |
| NG_027940.1:g.5982T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005618.4:c.235T>G MANE Select | NP_005609.3:p.Tyr79Asp |
| ENST00000366756.4:c.235T>G MANE Select | ENSP00000355718.3:p.Tyr79Asp |
| NM_005618.3:c.235T>G | NP_005609.3:p.Tyr79Asp |
| ENST00000366756.3:c.235T>G | ENSP00000355718.3:p.Tyr79Asp |
| XM_005266934.2:c.235T>G | XP_005266991.1:p.Tyr79Asp |
| XM_005266934.4:c.235T>G | XP_005266991.1:p.Tyr79Asp |
| XM_011535758.1:c.235T>G | XP_011534060.1:p.Tyr79Asp |