HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5227156A>G , CM000673.2:g.5227156A>G | GRCh38 |
NC_000011.9:g.5248386A>G , CM000673.1:g.5248386A>G | GRCh37 |
NC_000011.8:g.5204962A>G | NCBI36 |
NG_000007.3:g.70460T>C | |
NG_059281.1:g.4916T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.-135T>C | ENSP00000494175.1:n.-135T>C | |
ENST00000380315.2:c.-18-117T>C | ENSP00000369671.2:n.-18-117T>C |