Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146340676G>T , CM000667.2:g.146340676G>T | GRCh38 |
| NC_000005.9:g.145720239G>T , CM000667.1:g.145720239G>T | GRCh37 |
| NC_000005.8:g.145700432G>T | NCBI36 |
| NG_011885.1:g.6653G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002700.3:c.*232G>T MANE Select | NP_002691.1:n.*232G>T |
| ENST00000646991.2:c.*232G>T MANE Select | ENSP00000495718.1:n.*232G>T |