Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022651T>C , CM000663.2:g.17022651T>C | GRCh38 |
| NC_000001.10:g.17349146T>C , CM000663.1:g.17349146T>C | GRCh37 |
| NC_000001.9:g.17221733T>C | NCBI36 |
| NG_012340.1:g.36520A>G , LRG_316:g.36520A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463045.3:c.551A>G | ENSP00000481376.2:p.Tyr184Cys | |
| ENST00000491274.6:c.680A>G | ENSP00000480482.2:p.Tyr227Cys | |
| ENST00000375499.8:c.722A>G MANE Select | ENSP00000364649.3:p.Tyr241Cys | |
| ENST00000375499.7:c.722A>G | ENSP00000364649.3:p.Tyr241Cys | |
| ENST00000475049.5:n.147A>G | ||
| ENST00000485092.5:n.386A>G | ||
| ENST00000485515.5:n.656A>G | ||
| NM_003000.2:c.722A>G , LRG_316t1:c.722A>G | NP_002991.2:p.Tyr241Cys | |
| NM_003000.3:c.722A>G MANE Select | NP_002991.2:p.Tyr241Cys |