HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5227072A>C , CM000673.2:g.5227072A>C | GRCh38 |
NC_000011.9:g.5248302A>C , CM000673.1:g.5248302A>C | GRCh37 |
NC_000011.8:g.5204878A>C | NCBI36 |
NG_000007.3:g.70544T>G | |
NG_059281.1:g.5000T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.-51T>G | ENSP00000494175.1:n.-51T>G | |
ENST00000380315.2:c.-18-33T>G | ENSP00000369671.2:n.-18-33T>G | |
ENST00000485743.1:n.1T>G |