Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74685496T>C , CM000667.2:g.74685496T>C | GRCh38 |
| NC_000005.9:g.73981321T>C , CM000667.1:g.73981321T>C | GRCh37 |
| NC_000005.8:g.74017077T>C | NCBI36 |
| NG_009770.1:g.5353T>C | |
| NG_009770.2:g.50474T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000521.4:c.236T>C MANE Select | NP_000512.2:p.Ile79Thr |
| ENST00000261416.12:c.236T>C MANE Select | ENSP00000261416.7:p.Ile79Thr |
| NM_000521.3:c.236T>C | NP_000512.1:p.Ile79Thr |
| NM_001292004.1:c.-376-3832T>C | NP_001278933.1:n.-376-3832T>C |
| NM_001292004.2:c.-376-3832T>C | NP_001278933.1:n.-376-3832T>C |
| ENST00000261416.11:c.236T>C | ENSP00000261416.7:p.Ile79Thr |
| ENST00000511181.5:c.-376-3832T>C | ENSP00000426285.1:n.-376-3832T>C |
| ENST00000513079.5:n.301T>C | |
| ENST00000515528.1:n.291T>C |