HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73404213A>G , CM000666.2:g.73404213A>G | GRCh38 |
NC_000004.11:g.74269930A>G , CM000666.1:g.74269930A>G | GRCh37 |
NC_000004.10:g.74488794A>G | NCBI36 |
NG_009291.1:g.4959A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000441319.5:c.48-156A>G | ENSP00000392541.1:n.48-156A>G |