LDH info

Canonical Allele Identifier: CA124686
Gene: HBD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 15072
ClinVar RCV Id: RCV000016224
dbSNP Id: rs34975911

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234560A>G , CM000673.2:g.5234560A>G GRCh38
NC_000011.9:g.5255790A>G , CM000673.1:g.5255790A>G GRCh37
NC_000011.8:g.5212366A>G NCBI36
NG_000007.3:g.63056T>C
NG_063112.2:g.14098T>C

Transcript Alleles

HGVS Amino-acid change
NM_000519.3:c.-127T>C VV NP_000510.1:p.=
ENST00000380299.3:c.-127T>C ENSP00000369654.3:p.=
ENST00000429817.1:c.-97-30T>C ENSP00000393810.1:p.=