Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118110235T>C , CM000670.2:g.118110235T>C | GRCh38 |
| NC_000008.10:g.119122474T>C , CM000670.1:g.119122474T>C | GRCh37 |
| NC_000008.9:g.119191655T>C | NCBI36 |
| NG_007455.2:g.6585A>G , LRG_493:g.6585A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378204.7:c.812A>G MANE Select | ENSP00000367446.3:p.Tyr271Cys | |
| ENST00000436216.2:c.180A>G | ||
| ENST00000378204.6:c.812A>G | ENSP00000367446.2:p.Tyr271Cys | |
| ENST00000436216.1:c.180A>G | ||
| ENST00000437196.1:c.73+739A>G | ENSP00000407299.1:n.73+739A>G | |
| NM_000127.2:c.812A>G , LRG_493t1:c.812A>G | NP_000118.2:p.Tyr271Cys | |
| NM_000127.3:c.812A>G MANE Select | NP_000118.2:p.Tyr271Cys |