LDH info

Canonical Allele Identifier: CA204846
Gene: NTF4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 208763
ClinVar RCV Id: RCV000190785
dbSNP Id: rs797044939

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061477T>C , CM000681.2:g.49061477T>C GRCh38
NC_000019.9:g.49564734T>C , CM000681.1:g.49564734T>C GRCh37
NC_000019.8:g.54256546T>C NCBI36
NG_016289.1:g.7391A>G

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.521A>G VV NP_006170.1:p.Gln174Arg
XM_005258962.2:c.521A>G XP_005259019.1:p.Gln174Arg
XM_006723232.2:c.521A>G XP_006723295.1:p.Gln174Arg
XM_011527008.1:c.551A>G XP_011525310.1:p.Gln184Arg
XM_011527009.1:c.521A>G XP_011525311.1:p.Gln174Arg
XM_011527010.1:c.521A>G XP_011525312.1:p.Gln174Arg
XM_005258962.3:c.521A>G XP_005259019.1:p.Gln174Arg
XM_006723232.3:c.521A>G XP_006723295.1:p.Gln174Arg
XM_011527008.2:c.551A>G XP_011525310.1:p.Gln184Arg
XM_011527009.2:c.521A>G XP_011525311.1:p.Gln174Arg
XM_011527010.2:c.521A>G XP_011525312.1:p.Gln174Arg
XR_001753693.1:n.566A>G
XR_001753694.1:n.566A>G
ENST00000593537.1:n.521A>G ENSP00000469455.1:p.Gln174Arg
ENST00000599795.5:c.243+278A>G ENSP00000470689.1:p.=