HGVS | Genome Assembly |
---|---|
NC_000013.11:g.40644098T>C , CM000675.2:g.40644098T>C | GRCh38 |
NC_000013.10:g.41218235T>C , CM000675.1:g.41218235T>C | GRCh37 |
NC_000013.9:g.40116235T>C | NCBI36 |
NG_023244.1:g.27500A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379561.6:c.630+21485A>G MANE Select | ENSP00000368880.4:n.630+21485A>G | |
ENST00000655267.1:n.333+21485A>G | ||
ENST00000660760.1:n.296-10850A>G | ||
ENST00000379561.5:c.630+21485A>G | ENSP00000368880.4:n.630+21485A>G | |
NM_002015.3:c.630+21485A>G | NP_002006.2:n.630+21485A>G | |
XR_941536.1:n.1226+1241A>G | ||
NM_002015.4:c.630+21485A>G MANE Select | NP_002006.2:n.630+21485A>G |