Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.220126827G>C , CM000663.2:g.220126827G>C | GRCh38 |
| NC_000001.10:g.220300169G>C , CM000663.1:g.220300169G>C | GRCh37 |
| NC_000001.9:g.218366792G>C | NCBI36 |
| NG_041799.1:g.37715G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018060.4:c.1821G>C MANE Select | NP_060530.3:p.Trp607Cys |
| ENST00000366922.3:c.1821G>C MANE Select | ENSP00000355889.2:p.Trp607Cys |
| NM_018060.3:c.1821G>C | NP_060530.3:p.Trp607Cys |
| ENST00000366922.2:c.1821G>C | ENSP00000355889.2:p.Trp607Cys |
| ENST00000490891.1:n.205G>C |