HGVS | Genome Assembly |
---|---|
NC_000023.11:g.37804012G= , CM000685.2:g.37804012G= | GRCh38 |
NC_000023.10:g.37663265G= , CM000685.1:g.37663265G= | GRCh37 |
NC_000023.9:g.37548209G= | NCBI36 |
NG_009065.1:g.28996G= , LRG_53:g.28996G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696170.1:c.*542G= | ENSP00000512461.1:n.*542G= | |
ENST00000696171.1:c.937G= | ENSP00000512462.1:p.Ala313= | |
ENST00000378588.5:c.1033G= MANE Select | ENSP00000367851.4:p.Ala345= | |
ENST00000378588.4:c.1033G= | ENSP00000367851.4:p.Ala345= | |
ENST00000465127.1:c.171+378012G= | ENSP00000417050.1:n.171+378012G= | |
ENST00000492288.1:n.458G= | ||
NM_000397.3:c.1033G= , LRG_53t1:c.1033G= | NP_000388.2:p.Ala345= | |
XM_011543890.1:c.727G= | XP_011542192.1:p.Ala243= | |
NM_000397.4:c.1033G= MANE Select | NP_000388.2:p.Ala345= |