HGVS | Genome Assembly |
---|---|
NC_000013.11:g.40644141C= , CM000675.2:g.40644141C= | GRCh38 |
NC_000013.10:g.41218278C= , CM000675.1:g.41218278C= | GRCh37 |
NC_000013.9:g.40116278C= | NCBI36 |
NG_023244.1:g.27457G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379561.6:c.630+21442G= MANE Select | ENSP00000368880.4:n.630+21442G= | |
ENST00000655267.1:n.333+21442G= | ||
ENST00000660760.1:n.296-10893G= | ||
ENST00000379561.5:c.630+21442G= | ENSP00000368880.4:n.630+21442G= | |
NM_002015.3:c.630+21442G= | NP_002006.2:n.630+21442G= | |
XR_941536.1:n.1226+1198G= | ||
NM_002015.4:c.630+21442G= MANE Select | NP_002006.2:n.630+21442G= |