HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2621145T>A , CM000671.2:g.2621145T>A | GRCh38 |
NC_000009.11:g.2621145T>A , CM000671.1:g.2621145T>A | GRCh37 |
NC_000009.10:g.2611145T>A | NCBI36 |
NG_012741.1:g.4353T>A |
HGVS | Amino-acid Change | |
---|---|---|
NR_015375.2:n.274+955A>T |