Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70175014A>G , CM000679.2:g.70175014A>G | GRCh38 |
| NC_000017.10:g.68171155A>G , CM000679.1:g.68171155A>G | GRCh37 |
| NC_000017.9:g.65682750A>G | NCBI36 |
| NG_008798.1:g.10480A>G , LRG_328:g.10480A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.-26A>G MANE Select | ENSP00000243457.2:n.-26A>G | |
| ENST00000243457.3:c.-26A>G | ENSP00000243457.2:n.-26A>G | |
| ENST00000535240.1:c.-26A>G | ENSP00000441848.1:n.-26A>G | |
| NM_000891.2:c.-26A>G , LRG_328t1:c.-26A>G | NP_000882.1:n.-26A>G | |
| XM_011524779.1:c.-26A>G | XP_011523081.1:n.-26A>G | |
| NM_000891.3:c.-26A>G MANE Select | NP_000882.1:n.-26A>G |