LDH info

Canonical Allele Identifier: CA125559
Gene: HBA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 15631
ClinVar RCV Id: RCV000016898
dbSNP Id: rs41515649

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173216G>A , CM000678.2:g.173216G>A GRCh38
NC_000016.9:g.223215G>A , CM000678.1:g.223215G>A GRCh37
NC_000016.8:g.163215G>A NCBI36
NG_000006.1:g.34079G>A
NG_059186.1:g.1566G>A
NG_059271.1:g.5370G>A

Transcript Alleles

HGVS Amino-acid change
NM_000517.4:c.187G>A VV NP_000508.1:p.Val63Met
NM_000517.6:c.187G>A VV NP_000508.1:p.Val63Met
ENST00000251595.10:c.187G>A ENSP00000251595.6:p.Val63Met
ENST00000397806.1:c.91G>A ENSP00000380908.1:p.Val31Met
ENST00000482565.1:n.323G>A
ENST00000484216.1:n.156G>A