Canonical Allele Identifier: CA305302639
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs146559461
gnomAD v4: 19-11120151-A-C
MyVariant Identifiers: chr19:g.11230827A>C (hg19) chr19:g.11120151A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120151A>C , CM000681.2:g.11120151A>C GRCh38
NC_000019.9:g.11230827A>C , CM000681.1:g.11230827A>C GRCh37
NC_000019.8:g.11091827A>C NCBI36
NG_009060.1:g.35771A>C , LRG_274:g.35771A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2163A>C ENSP00000252444.6:p.Thr721=
ENST00000559340.2:c.1765A>C ENSP00000453696.2:p.Arg589=
ENST00000560467.2:c.1785A>C ENSP00000453513.2:p.Thr595=
ENST00000558518.6:c.1905A>C MANE Select ENSP00000454071.1:p.Thr635=
ENST00000252444.9:c.2159A>C
ENST00000455727.6:c.1401A>C ENSP00000397829.2:p.Thr467=
ENST00000535915.5:c.1782A>C ENSP00000440520.1:p.Thr594=
ENST00000545707.5:c.1524A>C ENSP00000437639.1:p.Thr508=
ENST00000557933.5:c.1905A>C ENSP00000453557.1:p.Thr635=
ENST00000558013.5:c.1905A>C ENSP00000453346.1:p.Thr635=
ENST00000558518.5:c.1905A>C ENSP00000454071.1:p.Thr635=
ENST00000559340.1:c.486A>C
NM_000527.4:c.1905A>C , LRG_274t1:c.1905A>C NP_000518.1:p.Thr635=
NM_001195798.1:c.1905A>C NP_001182727.1:p.Thr635=
NM_001195799.1:c.1782A>C NP_001182728.1:p.Thr594=
NM_001195800.1:c.1401A>C NP_001182729.1:p.Thr467=
NM_001195803.1:c.1524A>C NP_001182732.1:p.Thr508=
XM_011528010.1:c.1905A>C XP_011526312.1:p.Thr635=
XM_011528011.1:c.1524A>C XP_011526313.1:p.Thr508=
XR_244074.2:n.1915A>C
XM_011528010.2:c.1905A>C XP_011526312.1:p.Thr635=
XR_001753685.2:n.2022A>C
XR_001753686.2:n.1882A>C
NM_000527.5:c.1905A>C MANE Select NP_000518.1:p.Thr635=
NM_001195798.2:c.1905A>C NP_001182727.1:p.Thr635=
NM_001195799.2:c.1782A>C NP_001182728.1:p.Thr594=
NM_001195800.2:c.1401A>C NP_001182729.1:p.Thr467=
NM_001195803.2:c.1524A>C NP_001182732.1:p.Thr508=
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