Canonical Allele Identifier: CA631769771

Gene: LDLR

Linked Data

• dbSNP Id: rs1568618110
• gnomAD v2: 19-11238646-C-T
• gnomAD v4: 19-11127970-C-T
• MyVariant Identifiers: chr19:g.11238646C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11127970C>T , CM000681.2:g.11127970C>T	GRCh38
NC_000019.9:g.11238646C>T , CM000681.1:g.11238646C>T	GRCh37
NC_000019.8:g.11099646C>T	NCBI36
NG_009060.1:g.43590C>T , LRG_274:g.43590C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2570-38C>T	ENSP00000252444.6:n.2570-38C>T
ENST00000559340.2:c.*381-38C>T	ENSP00000453696.2:n.*381-38C>T
ENST00000560467.2:c.2192-38C>T	ENSP00000453513.2:n.2192-38C>T
ENST00000558518.6:c.2312-38C>T MANE Select	ENSP00000454071.1:n.2312-38C>T
ENST00000252444.9:c.2566-38C>T
ENST00000455727.6:c.1808-38C>T	ENSP00000397829.2:n.1808-38C>T
ENST00000535915.5:c.2189-38C>T	ENSP00000440520.1:n.2189-38C>T
ENST00000545707.5:c.1778-38C>T	ENSP00000437639.1:n.1778-38C>T
ENST00000557933.5:c.2312-38C>T	ENSP00000453557.1:n.2312-38C>T
ENST00000558013.5:c.2312-38C>T	ENSP00000453346.1:n.2312-38C>T
ENST00000558518.5:c.2312-38C>T	ENSP00000454071.1:n.2312-38C>T
ENST00000560628.1:n.108+316C>T
NM_000527.4:c.2312-38C>T , LRG_274t1:c.2312-38C>T	NP_000518.1:n.2312-38C>T
NM_001195798.1:c.2312-38C>T	NP_001182727.1:n.2312-38C>T
NM_001195799.1:c.2189-38C>T	NP_001182728.1:n.2189-38C>T
NM_001195800.1:c.1808-38C>T	NP_001182729.1:n.1808-38C>T
NM_001195803.1:c.1778-38C>T	NP_001182732.1:n.1778-38C>T
XM_011528010.1:c.2312-1543C>T	XP_011526312.1:n.2312-1543C>T
XM_011528011.1:c.1931-38C>T	XP_011526313.1:n.1931-38C>T
XR_244074.2:n.2322-38C>T
XM_011528010.2:c.2312-1543C>T	XP_011526312.1:n.2312-1543C>T
XR_001753685.2:n.2646-38C>T
XR_001753686.2:n.2289-38C>T
NM_000527.5:c.2312-38C>T MANE Select	NP_000518.1:n.2312-38C>T
NM_001195798.2:c.2312-38C>T	NP_001182727.1:n.2312-38C>T
NM_001195799.2:c.2189-38C>T	NP_001182728.1:n.2189-38C>T
NM_001195800.2:c.1808-38C>T	NP_001182729.1:n.1808-38C>T
NM_001195803.2:c.1778-38C>T	NP_001182732.1:n.1778-38C>T