dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.58497880C>A , CM000670.2:g.58497880C>A | GRCh38 |
| NC_000008.10:g.59410439C>A , CM000670.1:g.59410439C>A | GRCh37 |
| NC_000008.9:g.59572993C>A | NCBI36 |
| NG_007969.1:g.7283G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301645.4:c.321+349G>T MANE Select | ENSP00000301645.3:n.321+349G>T | |
| ENST00000301645.3:c.321+349G>T | ENSP00000301645.3:n.321+349G>T | |
| NM_000780.3:c.321+349G>T | NP_000771.2:n.321+349G>T | |
| XM_011517476.1:c.321+349G>T | XP_011515778.1:n.321+349G>T | |
| NM_000780.4:c.321+349G>T MANE Select | NP_000771.2:n.321+349G>T |