HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154191621T>G , CM000685.2:g.154191621T>G | GRCh38 |
NC_000023.10:g.153457112T>G , CM000685.1:g.153457112T>G | GRCh37 |
NG_011606.1:g.14028T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000595290.6:c.579-67T>G MANE Select | ENSP00000472316.1:n.579-67T>G | |
ENST00000595290.5:c.579-67T>G | ENSP00000472316.1:n.579-67T>G | |
ENST00000595330.1:n.588+1399T>G | ||
ENST00000596998.2:c.166-67T>G | ||
NM_000513.2:c.579-67T>G MANE Select | NP_000504.1:n.579-67T>G |