LDH info

Canonical Allele Identifier: CA126374
Gene: FGFR4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16326
ClinVar RCV Id: RCV000017723
dbSNP Id: rs351855

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093242G>A , CM000667.2:g.177093242G>A GRCh38
NC_000005.9:g.176520243G>A , CM000667.1:g.176520243G>A GRCh37
NC_000005.8:g.176452849G>A NCBI36
NG_012067.1:g.11323G>A

Transcript Alleles

HGVS Amino-acid change
NM_001291980.1:c.1097+65G>A VV NP_001278909.1:p.=
NM_002011.4:c.1162G>A VV NP_002002.3:p.Gly388Arg
NM_022963.3:c.1058-90G>A VV NP_075252.2:p.=
NM_213647.2:c.1162G>A VV NP_998812.1:p.Gly388Arg
XM_005265838.2:c.1162G>A XP_005265895.1:p.Gly388Arg
XM_011534464.1:c.1255G>A XP_011532766.1:p.Gly419Arg
XM_011534465.1:c.844G>A XP_011532767.1:p.Gly282Arg
XR_941090.1:n.1207G>A
NM_001354984.1:c.1162G>A VV NP_001341913.1:p.Gly388Arg
NM_213647.3:c.1162G>A VV MANE Preferred NP_998812.1:p.Gly388Arg
NM_001291980.2:c.1097+65G>A VV NP_001278909.1:p.=
NM_001354984.2:c.1162G>A VV NP_001341913.1:p.Gly388Arg
NM_002011.5:c.1162G>A VV NP_002002.3:p.Gly388Arg
ENST00000292408.8:c.1162G>A ENSP00000292408.4:p.Gly388Arg
ENST00000393637.5:c.1058-90G>A ENSP00000377254.1:p.=
ENST00000393648.6:c.1097+65G>A ENSP00000377259.2:p.=
ENST00000502906.5:c.1162G>A ENSP00000424960.1:p.Gly388Arg
ENST00000508139.1:n.466G>A
ENST00000511076.1:n.68G>A