HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2618969T>C , CM000671.2:g.2618969T>C | GRCh38 |
NC_000009.11:g.2618969T>C , CM000671.1:g.2618969T>C | GRCh37 |
NC_000009.10:g.2608969T>C | NCBI36 |
NG_012741.1:g.2177T>C |
HGVS | Amino-acid Change | |
---|---|---|
NR_015375.2:n.274+3131A>G |