HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196995758G= , CM000663.2:g.196995758G= | GRCh38 |
NC_000001.10:g.196964888G= , CM000663.1:g.196964888G= | GRCh37 |
NC_000001.9:g.195231511G= | NCBI36 |
NG_016365.1:g.23222G= , LRG_227:g.23222G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.394G= | ENSP00000514393.1:p.Gly132= | |
ENST00000699467.1:n.718G= | ||
ENST00000699468.1:c.-24-356G= | ENSP00000514394.1:n.-24-356G= | |
ENST00000256785.5:c.649G= MANE Select | ENSP00000256785.4:p.Gly217= | |
ENST00000256785.4:c.649G= | ENSP00000256785.4:p.Gly217= | |
NM_030787.3:c.649G= , LRG_227t1:c.649G= | NP_110414.1:p.Gly217= | |
XM_011510020.1:c.658G= | XP_011508322.1:p.Gly220= | |
XM_011510020.2:c.658G= | XP_011508322.1:p.Gly220= | |
NM_030787.4:c.649G= MANE Select | NP_110414.1:p.Gly217= |