Canonical Allele Identifier: CA4964430
Gene: VLDLR HGNC NCBI

Linked Data

dbSNP Id: rs761568886
gnomAD v2: 9-2635478-C-G
gnomAD v4: 9-2635478-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2635478C>G , CM000671.2:g.2635478C>G GRCh38
NC_000009.11:g.2635478C>G , CM000671.1:g.2635478C>G GRCh37
NC_000009.10:g.2625478C>G NCBI36
NG_012741.1:g.18686C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382096.6:c.108C>G ENSP00000371528.2:p.Ser36=
ENST00000382100.8:c.108C>G MANE Select ENSP00000371532.2:p.Ser36=
ENST00000679851.1:n.93C>G
ENST00000680021.1:n.308C>G
ENST00000680243.1:c.108C>G ENSP00000505911.1:p.Ser36=
ENST00000680746.1:c.108C>G ENSP00000505030.1:p.Ser36=
ENST00000680891.1:c.206C>G ENSP00000505167.1:p.Pro69Arg
ENST00000681306.1:c.108C>G ENSP00000506072.1:p.Ser36=
ENST00000681618.1:c.108C>G ENSP00000505773.1:p.Ser36=
ENST00000681644.1:c.206C>G ENSP00000505180.1:p.Pro69Arg
ENST00000681770.1:n.96C>G
ENST00000681806.1:c.108C>G ENSP00000505282.1:p.Ser36=
ENST00000382096.5:c.108C>G ENSP00000371528.1:p.Ser36=
ENST00000382099.2:c.108C>G ENSP00000371531.2:p.Ser36=
ENST00000382100.7:c.108C>G ENSP00000371532.2:p.Ser36=
NM_001018056.1:c.108C>G NP_001018066.1:p.Ser36=
NM_003383.3:c.108C>G NP_003374.3:p.Ser36=
XM_011518029.1:c.108C>G XP_011516331.1:p.Ser36=
NM_001018056.2:c.108C>G NP_001018066.1:p.Ser36=
NM_001322225.1:c.108C>G NP_001309154.1:p.Ser36=
NM_001322226.1:c.108C>G NP_001309155.1:p.Ser36=
NM_003383.4:c.108C>G NP_003374.3:p.Ser36=
XR_001746373.2:n.512C>G
XR_002956805.1:n.512C>G
NM_003383.5:c.108C>G MANE Select NP_003374.3:p.Ser36=
NM_001018056.3:c.108C>G NP_001018066.1:p.Ser36=
NM_001322225.2:c.108C>G NP_001309154.1:p.Ser36=
NM_001322226.2:c.108C>G NP_001309155.1:p.Ser36=