Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.122077684G>A , CM000667.2:g.122077684G>A | GRCh38 |
| NC_000005.9:g.121413379G>A , CM000667.1:g.121413379G>A | GRCh37 |
| NC_000005.8:g.121441278G>A | NCBI36 |
| NG_008722.1:g.5677C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002317.7:c.302C>T MANE Select | NP_002308.2:p.Ala101Val |
| ENST00000231004.5:c.302C>T MANE Select | ENSP00000231004.4:p.Ala101Val |
| NM_002317.5:c.302C>T | NP_002308.2:p.Ala101Val |
| NM_002317.6:c.302C>T | NP_002308.2:p.Ala101Val |
| ENST00000231004.4:c.302C>T | ENSP00000231004.4:p.Ala101Val |
| ENST00000639739.2:c.302C>T | ENSP00000492324.2:p.Ala101Val |