HGVS | Genome Assembly |
---|---|
NC_000017.11:g.50199235G>T , CM000679.2:g.50199235G>T | GRCh38 |
NC_000017.10:g.48276596G>T , CM000679.1:g.48276596G>T | GRCh37 |
NC_000017.9:g.45631595G>T | NCBI36 |
NG_007400.1:g.7405C>A , LRG_1:g.7405C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225964.10:c.462C>A MANE Select | ENSP00000225964.6:p.Gly154= | |
ENST00000225964.9:c.462C>A | ENSP00000225964.5:p.Gly154= | |
NM_000088.3:c.462C>A , LRG_1t1:c.462C>A | NP_000079.2:p.Gly154= | |
XM_005257058.3:c.462C>A | XP_005257115.2:p.Gly154= | |
XM_005257059.3:c.462C>A | XP_005257116.2:p.Gly154= | |
XM_011524341.1:c.462C>A | XP_011522643.1:p.Gly154= | |
XM_005257058.4:c.462C>A | XP_005257115.2:p.Gly154= | |
XM_005257059.4:c.462C>A | XP_005257116.2:p.Gly154= | |
NM_000088.4:c.462C>A MANE Select | NP_000079.2:p.Gly154= |