Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31859734G>A , CM000668.2:g.31859734G>A | GRCh38 |
| NC_000006.11:g.31827511G>A , CM000668.1:g.31827511G>A | GRCh37 |
| NC_000006.10:g.31935490G>A | NCBI36 |
| NG_008201.1:g.8199C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.1233C>T MANE Select | ENSP00000364782.4:p.Val411= | |
| ENST00000677054.1:n.2572C>T | ||
| ENST00000677512.1:n.1510C>T | ||
| ENST00000678869.1:n.1821C>T | ||
| ENST00000375631.4:c.1233C>T | ENSP00000364782.4:p.Val411= | |
| ENST00000480384.1:n.1532C>T | ||
| ENST00000491768.5:c.*343C>T | ENSP00000433127.1:n.*343C>T | |
| ENST00000495807.1:n.2541C>T | ||
| NM_000434.3:c.1233C>T | NP_000425.1:p.Val411= | |
| NM_000434.4:c.1233C>T MANE Select | NP_000425.1:p.Val411= |