HGVS | Genome Assembly |
---|---|
NC_000005.10:g.132868735C>G , CM000667.2:g.132868735C>G | GRCh38 |
NC_000005.9:g.132204427C>G , CM000667.1:g.132204427C>G | GRCh37 |
NC_000005.8:g.132232326C>G | NCBI36 |
NG_012221.1:g.7109C>G | |
NG_047051.1:g.3150G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378670.8:c.*1153C>G MANE Select | ENSP00000367939.3:n.*1153C>G | |
NM_014402.4:c.*1153C>G | NP_055217.2:n.*1153C>G | |
NM_014402.5:c.*1153C>G MANE Select | NP_055217.2:n.*1153C>G |