LDH info

Canonical Allele Identifier: CA123709
Gene: NTF4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14019
ClinVar RCV Id: RCV000015062
dbSNP Id: rs121918428

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061381C>T , CM000681.2:g.49061381C>T GRCh38
NC_000019.9:g.49564638C>T , CM000681.1:g.49564638C>T GRCh37
NC_000019.8:g.54256450C>T NCBI36
NG_016289.1:g.7487G>A

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.617G>A VV NP_006170.1:p.Arg206Gln
XM_005258962.2:c.617G>A XP_005259019.1:p.Arg206Gln
XM_006723232.2:c.617G>A XP_006723295.1:p.Arg206Gln
XM_011527008.1:c.647G>A XP_011525310.1:p.Arg216Gln
XM_011527009.1:c.617G>A XP_011525311.1:p.Arg206Gln
XM_011527010.1:c.617G>A XP_011525312.1:p.Arg206Gln
XM_005258962.3:c.617G>A XP_005259019.1:p.Arg206Gln
XM_006723232.3:c.617G>A XP_006723295.1:p.Arg206Gln
XM_011527008.2:c.647G>A XP_011525310.1:p.Arg216Gln
XM_011527009.2:c.617G>A XP_011525311.1:p.Arg206Gln
XM_011527010.2:c.617G>A XP_011525312.1:p.Arg206Gln
XR_001753693.1:n.662G>A
XR_001753694.1:n.662G>A
ENST00000593537.1:n.617G>A ENSP00000469455.1:p.Arg206Gln
ENST00000599795.5:c.243+374G>A ENSP00000470689.1:p.=