HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64750355C>G , CM000673.2:g.64750355C>G | GRCh38 |
NC_000011.9:g.64517827C>G , CM000673.1:g.64517827C>G | GRCh37 |
NC_000011.8:g.64274403C>G | NCBI36 |
NG_007574.1:g.102G>C , LRG_100:g.102G>C | |
NG_013018.1:g.15361G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.2177+21G>C MANE Select | ENSP00000164139.3:n.2177+21G>C | |
ENST00000164139.3:c.2177+21G>C | ENSP00000164139.3:n.2177+21G>C | |
ENST00000377432.7:c.1913+21G>C | ENSP00000366650.3:n.1913+21G>C | |
NM_001164716.1:c.1913+21G>C | NP_001158188.1:n.1913+21G>C | |
NM_005609.2:c.2177+21G>C | NP_005600.1:n.2177+21G>C | |
NM_005609.3:c.2177+21G>C | NP_005600.1:n.2177+21G>C | |
NM_005609.4:c.2177+21G>C MANE Select | NP_005600.1:n.2177+21G>C |