Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146340681A>T , CM000667.2:g.146340681A>T | GRCh38 |
| NC_000005.9:g.145720244A>T , CM000667.1:g.145720244A>T | GRCh37 |
| NC_000005.8:g.145700437A>T | NCBI36 |
| NG_011885.1:g.6658A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002700.3:c.*237A>T MANE Select | NP_002691.1:n.*237A>T |
| ENST00000646991.2:c.*237A>T MANE Select | ENSP00000495718.1:n.*237A>T |