Canonical Allele Identifier: CA16602289
Gene: LDLR HGNC NCBI
LDLR-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375772
ClinVar RCV Id: RCV000417306
dbSNP Id: rs1057519650

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11089450A>G , CM000681.2:g.11089450A>G GRCh38
NC_000019.9:g.11200126A>G , CM000681.1:g.11200126A>G GRCh37
NC_000019.8:g.11061126A>G NCBI36
NG_009060.1:g.5070A>G , LRG_274:g.5070A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559340.2:c.-99A>G (LDLR) ENSP00000453696.2:n.-99A>G
ENST00000558518.5:c.-99A>G (LDLR) ENSP00000454071.1:n.-99A>G
NM_000527.4:c.-99A>G , LRG_274t1:c.-99A>G (LDLR) NP_000518.1:n.-99A>G
NM_001195798.1:c.-99A>G (LDLR) NP_001182727.1:n.-99A>G
NM_001195799.1:c.-99A>G (LDLR) NP_001182728.1:n.-99A>G
NM_001195800.1:c.-99A>G (LDLR) NP_001182729.1:n.-99A>G
NM_001195803.1:c.-99A>G (LDLR) NP_001182732.1:n.-99A>G
XM_011528010.1:c.-99A>G (LDLR) XP_011526312.1:n.-99A>G
XM_011528011.1:c.-99A>G (LDLR) XP_011526313.1:n.-99A>G
XR_244074.2:n.52A>G (LDLR)
XM_011528010.2:c.-99A>G (LDLR) XP_011526312.1:n.-99A>G
XR_001753685.2:n.19A>G (LDLR)
XR_001753686.2:n.19A>G (LDLR)
NR_163945.1:n.210T>C (LDLR-AS1)