HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996095A= , CM000663.2:g.196996095A= | GRCh38 |
NC_000001.10:g.196965225A= , CM000663.1:g.196965225A= | GRCh37 |
NC_000001.9:g.195231848A= | NCBI36 |
NG_016365.1:g.23559A= , LRG_227:g.23559A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.609A= | ENSP00000514393.1:p.Gln203= | |
ENST00000699467.1:n.933A= | ||
ENST00000699468.1:c.-24-19A= | ENSP00000514394.1:n.-24-19A= | |
ENST00000256785.5:c.864A= MANE Select | ENSP00000256785.4:p.Gln288= | |
ENST00000256785.4:c.864A= | ENSP00000256785.4:p.Gln288= | |
NM_030787.3:c.864A= , LRG_227t1:c.864A= | NP_110414.1:p.Gln288= | |
XM_011510020.1:c.873A= | XP_011508322.1:p.Gln291= | |
XM_011510020.2:c.873A= | XP_011508322.1:p.Gln291= | |
NM_030787.4:c.864A= MANE Select | NP_110414.1:p.Gln288= |