Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81648700C>T , CM000665.2:g.81648700C>T | GRCh38 |
| NC_000003.11:g.81697851C>T , CM000665.1:g.81697851C>T | GRCh37 |
| NC_000003.10:g.81780541C>T | NCBI36 |
| NG_011810.1:g.118101G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.691+156G>A MANE Select | ENSP00000410833.2:n.691+156G>A | |
| ENST00000429644.6:c.691+156G>A | ENSP00000410833.2:n.691+156G>A | |
| ENST00000489715.1:c.568+156G>A | ENSP00000419638.1:n.568+156G>A | |
| ENST00000498468.1:n.219+156G>A | ||
| NM_000158.3:c.691+156G>A | NP_000149.3:n.691+156G>A | |
| NM_000158.4:c.691+156G>A MANE Select | NP_000149.4:n.691+156G>A |