Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63966221A>G , CM000679.2:g.63966221A>G | GRCh38 |
| NC_000017.10:g.62043581A>G , CM000679.1:g.62043581A>G | GRCh37 |
| NC_000017.9:g.59397313A>G | NCBI36 |
| NG_011699.1:g.11698T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.1123T>C MANE Select | NP_000325.4:p.Cys375Arg |
| ENST00000435607.3:c.1123T>C MANE Select | ENSP00000396320.1:p.Cys375Arg |
| ENST00000578147.5:c.1123T>C | ENSP00000463963.1:p.Cys375Arg |
| XM_005257566.3:c.1123T>C | XP_005257623.1:p.Cys375Arg |
| XR_001752969.1:n.1554-284A>G | |
| XR_001752970.1:n.506-284A>G | |
| XR_934910.1:n.277-284A>G | |
| XR_934910.2:n.1429-284A>G |