HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315056T>C , CM000667.2:g.159315056T>C | GRCh38 |
NC_000005.9:g.158742064T>C , CM000667.1:g.158742064T>C | GRCh37 |
NC_000005.8:g.158674642T>C | NCBI36 |
NG_009618.1:g.20418A>G , LRG_71:g.20418A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.*1045A>G | ENSP00000512849.1:n.*1045A>G | |
ENST00000696751.1:c.*1527A>G | ENSP00000512850.1:n.*1527A>G | |
ENST00000231228.3:c.*1045A>G MANE Select | ENSP00000231228.2:n.*1045A>G | |
ENST00000231228.2:c.*1045A>G | ENSP00000231228.2:n.*1045A>G | |
NM_002187.2:c.*1045A>G , LRG_71t1:c.*1045A>G | NP_002178.2:n.*1045A>G | |
XR_941138.1:n.364-162T>C | ||
XR_941138.2:n.431-162T>C | ||
NM_002187.3:c.*1045A>G MANE Select | NP_002178.2:n.*1045A>G |