Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860150G>A , CM000668.2:g.31860150G>A | GRCh38 |
| NC_000006.11:g.31827927G>A , CM000668.1:g.31827927G>A | GRCh37 |
| NC_000006.10:g.31935906G>A | NCBI36 |
| NG_008201.1:g.7783C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000434.4:c.913C>T MANE Select | NP_000425.1:p.Arg305Cys |
| ENST00000375631.5:c.913C>T MANE Select | ENSP00000364782.4:p.Arg305Cys |
| NM_000434.3:c.913C>T | NP_000425.1:p.Arg305Cys |
| ENST00000375631.4:c.913C>T | ENSP00000364782.4:p.Arg305Cys |
| ENST00000480384.1:n.1116C>T | |
| ENST00000491768.5:c.*23C>T | ENSP00000433127.1:n.*23C>T |
| ENST00000495807.1:n.2221C>T | |
| ENST00000677054.1:n.2156C>T | |
| ENST00000677512.1:n.1195C>T | |
| ENST00000678869.1:n.1501C>T |