Canonical Allele Identifier: CA207070
Gene: VLDLR HGNC NCBI
VLDLR-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212557
ClinVar RCV Id: RCV000193524
dbSNP Id: rs797046092

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2622191T>C , CM000671.2:g.2622191T>C GRCh38
NC_000009.11:g.2622191T>C , CM000671.1:g.2622191T>C GRCh37
NC_000009.10:g.2612191T>C NCBI36
NG_012741.1:g.5399T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382096.6:c.2T>C (VLDLR)
ENST00000382100.8:c.2T>C (VLDLR)
ENST00000680243.1:c.2T>C (VLDLR)
ENST00000680746.1:c.2T>C (VLDLR)
ENST00000680891.1:c.2T>C (VLDLR)
ENST00000681306.1:c.2T>C (VLDLR)
ENST00000681618.1:c.2T>C (VLDLR)
ENST00000681644.1:c.2T>C (VLDLR)
ENST00000681806.1:c.2T>C (VLDLR)
ENST00000382096.5:c.2T>C (VLDLR)
ENST00000382099.2:c.2T>C (VLDLR)
ENST00000382100.7:c.2T>C (VLDLR)
NM_001018056.1:c.2T>C (VLDLR)
NM_003383.3:c.2T>C (VLDLR)
NR_015375.2:n.183A>G (VLDLR-AS1)
XM_011518029.1:c.2T>C (VLDLR)
NM_001018056.2:c.2T>C (VLDLR)
NM_001322225.1:c.2T>C (VLDLR)
NM_001322226.1:c.2T>C (VLDLR)
NM_003383.4:c.2T>C (VLDLR)
XR_001746373.2:n.406T>C (VLDLR)
XR_002956805.1:n.406T>C (VLDLR)
NM_003383.5:c.2T>C (VLDLR)
NM_001018056.3:c.2T>C (VLDLR)
NM_001322225.2:c.2T>C (VLDLR)
NM_001322226.2:c.2T>C (VLDLR)