Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008209A>G , CM000666.2:g.88008209A>G | GRCh38 |
| NC_000004.11:g.88929361A>G , CM000666.1:g.88929361A>G | GRCh37 |
| NC_000004.10:g.89148385A>G | NCBI36 |
| NG_008604.1:g.5542A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.476A>G MANE Select | ENSP00000237596.2:p.Asp159Gly | |
| ENST00000237596.6:c.476A>G | ENSP00000237596.2:p.Asp159Gly | |
| NM_000297.3:c.476A>G | NP_000288.1:p.Asp159Gly | |
| XM_011532028.1:c.476A>G | XP_011530330.1:p.Asp159Gly | |
| XR_244632.2:n.571A>G | ||
| NR_156488.1:n.563A>G | ||
| XM_011532028.2:c.476A>G | XP_011530330.1:p.Asp159Gly | |
| NM_000297.4:c.476A>G MANE Select | NP_000288.1:p.Asp159Gly | |
| NR_156488.2:n.575A>G |