LDH info

Canonical Allele Identifier: CA8070132
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 417864
dbSNP Id: rs202114767

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56904402G>A , CM000678.2:g.56904402G>A GRCh38
NC_000016.9:g.56938314G>A , CM000678.1:g.56938314G>A GRCh37
NC_000016.8:g.55495815G>A NCBI36
NG_009386.1:g.44196G>A

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.2891G>A VV NP_000330.2:p.Arg964Gln
NM_001126107.1:c.2888G>A VV NP_001119579.1:p.Arg963Gln
NM_001126108.1:c.2864G>A VV NP_001119580.1:p.Arg955Gln
XM_005256119.1:c.2861G>A XP_005256176.1:p.Arg954Gln
XM_005256119.2:c.2861G>A XP_005256176.1:p.Arg954Gln
ENST00000262502.5:c.2861G>A ENSP00000262502.5:p.Arg954Gln
ENST00000438926.6:c.2891G>A ENSP00000402152.2:p.Arg964Gln
ENST00000563236.5:c.2864G>A ENSP00000456149.1:p.Arg955Gln
ENST00000566786.5:c.2888G>A ENSP00000457552.1:p.Arg963Gln
ENST00000569002.1:n.295G>A