LDH info

Canonical Allele Identifier: CA10610324
Gene: AGT HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 296090
ClinVar RCV Id: RCV000262949
dbSNP Id: rs5051

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230714126C>T , CM000663.2:g.230714126C>T GRCh38
NC_000001.10:g.230849872C>T , CM000663.1:g.230849872C>T GRCh37
NC_000001.9:g.228916495C>T NCBI36
NG_008836.1:g.5465G>A
NG_008836.2:g.5465G>A

Transcript Alleles

HGVS Amino-acid change
NM_000029.3:c.-44G>A VV NP_000020.1:p.=
ENST00000366667.4:c.-44G>A ENSP00000355627.4:p.=