HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022691C>A , CM000663.2:g.17022691C>A | GRCh38 |
NC_000001.10:g.17349186C>A , CM000663.1:g.17349186C>A | GRCh37 |
NC_000001.9:g.17221773C>A | NCBI36 |
NG_012340.1:g.36480G>T , LRG_316:g.36480G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.511G>T | ENSP00000481376.2:p.Glu171Ter | |
ENST00000491274.6:c.640G>T | ENSP00000480482.2:p.Glu214Ter | |
ENST00000375499.8:c.682G>T MANE Select | ENSP00000364649.3:p.Glu228Ter | |
ENST00000375499.7:c.682G>T | ENSP00000364649.3:p.Glu228Ter | |
ENST00000475049.5:n.107G>T | ||
ENST00000485092.5:n.346G>T | ||
ENST00000485515.5:n.616G>T | ||
NM_003000.2:c.682G>T , LRG_316t1:c.682G>T | NP_002991.2:p.Glu228Ter | |
NM_003000.3:c.682G>T MANE Select | NP_002991.2:p.Glu228Ter |