dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.70895776G>C , CM000674.2:g.70895776G>C | GRCh38 |
| NC_000012.11:g.71289556G>C , CM000674.1:g.71289556G>C | GRCh37 |
| NC_000012.10:g.69575823G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283228.7:c.59-2799C>G MANE Select | ENSP00000283228.2:n.59-2799C>G | |
| ENST00000283228.6:c.59-2799C>G | ENSP00000283228.2:n.59-2799C>G | |
| NM_002849.3:c.59-2799C>G | NP_002840.2:n.59-2799C>G | |
| XM_011538615.1:c.35-2799C>G | XP_011536917.1:n.35-2799C>G | |
| XM_011538616.1:c.59-2799C>G | XP_011536918.1:n.59-2799C>G | |
| XR_944652.1:n.447-2799C>G | ||
| XM_011538615.2:c.35-2799C>G | XP_011536917.1:n.35-2799C>G | |
| XR_001748830.1:n.401-2799C>G | ||
| NM_002849.4:c.59-2799C>G MANE Select | NP_002840.2:n.59-2799C>G |