LDH info

Canonical Allele Identifier: CA128555
Gene: SLC6A3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 29685
dbSNP Id: rs431905504

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1411242C>T , CM000667.2:g.1411242C>T GRCh38
NC_000005.9:g.1411357C>T , CM000667.1:g.1411357C>T GRCh37
NC_000005.8:g.1464357C>T NCBI36
NG_015885.1:g.39187G>A

Transcript Alleles

HGVS Amino-acid change
NM_001044.4:c.1269+1G>A VV NP_001035.1:p.=
NM_001044.5:c.1269+1G>A VV MANE Preferred NP_001035.1:p.=
ENST00000270349.11:c.1269+1G>A ENSP00000270349.9:p.=