HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99851540G>A , CM000672.2:g.99851540G>A | GRCh38 |
NC_000010.10:g.101611297G>A , CM000672.1:g.101611297G>A | GRCh37 |
NC_000010.9:g.101601287G>A | NCBI36 |
NG_011798.1:g.73835G>A | |
NG_011798.2:g.73943G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647814.1:c.4547G>A MANE Select | ENSP00000497274.1:p.Gly1516Asp | |
ENST00000648523.1:c.617G>A | ||
ENST00000370449.8:c.4547G>A | ENSP00000359478.4:p.Gly1516Asp | |
NM_000392.4:c.4547G>A | NP_000383.1:p.Gly1516Asp | |
XM_006717630.2:c.3851G>A | XP_006717693.1:p.Gly1284Asp | |
NM_000392.5:c.4547G>A MANE Select | NP_000383.2:p.Gly1516Asp | |
XM_006717630.3:c.3851G>A | XP_006717693.1:p.Gly1284Asp |