Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74689359T>C , CM000667.2:g.74689359T>C | GRCh38 |
| NC_000005.9:g.73985184T>C , CM000667.1:g.73985184T>C | GRCh37 |
| NC_000005.8:g.74020940T>C | NCBI36 |
| NG_009770.1:g.9216T>C | |
| NG_009770.2:g.54337T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261416.12:c.331T>C MANE Select | ENSP00000261416.7:p.Trp111Arg | |
| ENST00000261416.11:c.331T>C | ENSP00000261416.7:p.Trp111Arg | |
| ENST00000511181.5:c.-345T>C | ENSP00000426285.1:n.-345T>C | |
| ENST00000513079.5:n.396T>C | ||
| ENST00000515528.1:n.386T>C | ||
| NM_000521.3:c.331T>C | NP_000512.1:p.Trp111Arg | |
| NM_001292004.1:c.-345T>C | NP_001278933.1:n.-345T>C | |
| NM_000521.4:c.331T>C MANE Select | NP_000512.2:p.Trp111Arg | |
| NM_001292004.2:c.-345T>C | NP_001278933.1:n.-345T>C |