LDH info

Canonical Allele Identifier: CA123707
Gene: NTF4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14018
ClinVar RCV Id: RCV000015061
dbSNP Id: rs121918427

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061382G>A , CM000681.2:g.49061382G>A GRCh38
NC_000019.9:g.49564639G>A , CM000681.1:g.49564639G>A GRCh37
NC_000019.8:g.54256451G>A NCBI36
NG_016289.1:g.7486C>T

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.616C>T VV NP_006170.1:p.Arg206Trp
XM_005258962.2:c.616C>T XP_005259019.1:p.Arg206Trp
XM_006723232.2:c.616C>T XP_006723295.1:p.Arg206Trp
XM_011527008.1:c.646C>T XP_011525310.1:p.Arg216Trp
XM_011527009.1:c.616C>T XP_011525311.1:p.Arg206Trp
XM_011527010.1:c.616C>T XP_011525312.1:p.Arg206Trp
XM_005258962.3:c.616C>T XP_005259019.1:p.Arg206Trp
XM_006723232.3:c.616C>T XP_006723295.1:p.Arg206Trp
XM_011527008.2:c.646C>T XP_011525310.1:p.Arg216Trp
XM_011527009.2:c.616C>T XP_011525311.1:p.Arg206Trp
XM_011527010.2:c.616C>T XP_011525312.1:p.Arg206Trp
XR_001753693.1:n.661C>T
XR_001753694.1:n.661C>T
ENST00000593537.1:n.616C>T ENSP00000469455.1:p.Arg206Trp
ENST00000599795.5:c.243+373C>T ENSP00000470689.1:p.=