LDH info

Canonical Allele Identifier: CA6476722
Gene: SLCO1B1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37346
dbSNP Id: rs4149056

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178615T>C , CM000674.2:g.21178615T>C GRCh38
NC_000012.11:g.21331549T>C , CM000674.1:g.21331549T>C GRCh37
NC_000012.10:g.21222816T>C NCBI36
NG_011745.1:g.52422T>C , LRG_1022:g.52422T>C

Transcript Alleles

HGVS Amino-acid change
NM_006446.4:c.521T>C , LRG_1022t1:c.521T>C NP_006437.3:p.Val174Ala
NM_006446.5:c.521T>C VV NP_006437.3:p.Val174Ala
ENST00000256958.2:c.521T>C ENSP00000256958.2:p.Val174Ala