LDH info

Canonical Allele Identifier: CA149713
Gene: SLC6A3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 97016
ClinVar RCV Id: RCV000083262
dbSNP Id: rs431905514

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416097C>T , CM000667.2:g.1416097C>T GRCh38
NC_000005.9:g.1416212C>T , CM000667.1:g.1416212C>T GRCh37
NC_000005.8:g.1469212C>T NCBI36
NG_015885.1:g.34332G>A

Transcript Alleles

HGVS Amino-acid change
NM_001044.4:c.1031+1G>A VV NP_001035.1:p.=
NM_001044.5:c.1031+1G>A VV MANE Preferred NP_001035.1:p.=
ENST00000270349.11:c.1031+1G>A ENSP00000270349.9:p.=
ENST00000511750.1:n.481+1G>A