Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.175443193C>A , CM000667.2:g.175443193C>A | GRCh38 |
| NC_000005.9:g.174870196C>A , CM000667.1:g.174870196C>A | GRCh37 |
| NC_000005.8:g.174802802C>A | NCBI36 |
| NG_011802.1:g.5968G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000794.5:c.-94G>T MANE Select | NP_000785.1:n.-94G>T |
| ENST00000393752.3:c.-94G>T MANE Select | ENSP00000377353.1:n.-94G>T |
| NM_000794.3:c.-94G>T | NP_000785.1:n.-94G>T |
| NM_000794.4:c.-94G>T | NP_000785.1:n.-94G>T |
| ENST00000393752.2:c.-94G>T | ENSP00000377353.1:n.-94G>T |