HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73404170G>A , CM000666.2:g.73404170G>A | GRCh38 |
NC_000004.11:g.74269887G>A , CM000666.1:g.74269887G>A | GRCh37 |
NC_000004.10:g.74488751G>A | NCBI36 |
NG_009291.1:g.4916G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000441319.5:c.48-199G>A | ENSP00000392541.1:n.48-199G>A |