HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157626G>C , CM000681.2:g.55157626G>C | GRCh38 |
NC_000019.9:g.55668994G>C , CM000681.1:g.55668994G>C | GRCh37 |
NC_000019.8:g.60360806G>C | NCBI36 |
NG_007866.2:g.5107C>G , LRG_432:g.5107C>G | |
NG_032759.1:g.14097C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.-37C>G MANE Select | ENSP00000341838.5:n.-37C>G | |
ENST00000665070.1:c.-37C>G | ENSP00000499482.1:n.-37C>G | |
ENST00000344887.9:c.-37C>G | ENSP00000341838.5:n.-37C>G | |
ENST00000586446.1:n.107C>G | ||
ENST00000587176.5:n.148C>G | ||
ENST00000587871.1:c.584C>G | ||
ENST00000590463.1:n.91C>G | ||
NM_000363.4:c.-37C>G , LRG_432t1:c.-37C>G | NP_000354.4:n.-37C>G | |
NM_000363.5:c.-37C>G MANE Select | NP_000354.4:n.-37C>G |