Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81642522C>T , CM000665.2:g.81642522C>T | GRCh38 |
| NC_000003.11:g.81691673C>T , CM000665.1:g.81691673C>T | GRCh37 |
| NC_000003.10:g.81774363C>T | NCBI36 |
| NG_011810.1:g.124279G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.992+259G>A MANE Select | NP_000149.4:n.992+259G>A |
| ENST00000429644.7:c.992+259G>A MANE Select | ENSP00000410833.2:n.992+259G>A |
| NM_000158.3:c.992+259G>A | NP_000149.3:n.992+259G>A |
| ENST00000429644.6:c.992+259G>A | ENSP00000410833.2:n.992+259G>A |
| ENST00000489715.1:c.869+259G>A | ENSP00000419638.1:n.869+259G>A |