LDH info

Canonical Allele Identifier: CA122783
Gene: ATP1A2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12921
ClinVar RCV Id: RCV000013784
dbSNP Id: rs28934002

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160128767C>A , CM000663.2:g.160128767C>A GRCh38
NC_000001.10:g.160098557C>A , CM000663.1:g.160098557C>A GRCh37
NC_000001.9:g.158365181C>A NCBI36
NG_008014.1:g.18010C>A , LRG_6:g.18010C>A

Transcript Alleles

HGVS Amino-acid change
NM_000702.3:c.1133C>A VV NP_000693.1:p.Thr378Asn
ENST00000361216.7:c.1133C>A ENSP00000354490.3:p.Thr378Asn
ENST00000392233.7:c.1133C>A ENSP00000376066.3:p.Thr378Asn
ENST00000447527.1:n.265C>A
ENST00000472488.5:n.1236C>A