Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860176T>C , CM000668.2:g.31860176T>C | GRCh38 |
| NC_000006.11:g.31827953T>C , CM000668.1:g.31827953T>C | GRCh37 |
| NC_000006.10:g.31935932T>C | NCBI36 |
| NG_008201.1:g.7757A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000434.4:c.887A>G MANE Select | NP_000425.1:p.Tyr296Cys |
| ENST00000375631.5:c.887A>G MANE Select | ENSP00000364782.4:p.Tyr296Cys |
| NM_000434.3:c.887A>G | NP_000425.1:p.Tyr296Cys |
| ENST00000375631.4:c.887A>G | ENSP00000364782.4:p.Tyr296Cys |
| ENST00000480384.1:n.1090A>G | |
| ENST00000491768.5:c.801A>G | ENSP00000433127.1:p.Leu267= |
| ENST00000495807.1:n.2195A>G | |
| ENST00000677054.1:n.2130A>G | |
| ENST00000677512.1:n.1169A>G | |
| ENST00000678869.1:n.1475A>G |