Canonical Allele Identifier: CA631764377

Gene: LDLR

Linked Data

• dbSNP Id: rs1203928026
• gnomAD v2: 19-11218195-G-C
• gnomAD v3: 19-11107519-G-C
• gnomAD v4: 19-11107519-G-C
• MyVariant Identifiers: chr19:g.11218195G>C (hg19) ; chr19:g.11107519G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107519G>C , CM000681.2:g.11107519G>C	GRCh38
NC_000019.9:g.11218195G>C , CM000681.1:g.11218195G>C	GRCh37
NC_000019.8:g.11079195G>C	NCBI36
NG_009060.1:g.23139G>C , LRG_274:g.23139G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1198+5G>C	ENSP00000252444.6:n.1198+5G>C
ENST00000559340.2:c.940+5G>C	ENSP00000453696.2:n.940+5G>C
ENST00000560467.2:c.940+5G>C	ENSP00000453513.2:n.940+5G>C
ENST00000558518.6:c.940+5G>C MANE Select	ENSP00000454071.1:n.940+5G>C
ENST00000252444.9:c.1194+5G>C
ENST00000455727.6:c.436+5G>C	ENSP00000397829.2:n.436+5G>C
ENST00000535915.5:c.817+5G>C	ENSP00000440520.1:n.817+5G>C
ENST00000545707.5:c.559+5G>C	ENSP00000437639.1:n.559+5G>C
ENST00000557933.5:c.940+5G>C	ENSP00000453557.1:n.940+5G>C
ENST00000558013.5:c.940+5G>C	ENSP00000453346.1:n.940+5G>C
ENST00000558518.5:c.940+5G>C	ENSP00000454071.1:n.940+5G>C
ENST00000560467.1:c.540+5G>C
NM_000527.4:c.940+5G>C , LRG_274t1:c.940+5G>C	NP_000518.1:n.940+5G>C
NM_001195798.1:c.940+5G>C	NP_001182727.1:n.940+5G>C
NM_001195799.1:c.817+5G>C	NP_001182728.1:n.817+5G>C
NM_001195800.1:c.436+5G>C	NP_001182729.1:n.436+5G>C
NM_001195803.1:c.559+5G>C	NP_001182732.1:n.559+5G>C
XM_011528010.1:c.940+5G>C	XP_011526312.1:n.940+5G>C
XM_011528011.1:c.559+5G>C	XP_011526313.1:n.559+5G>C
XR_244074.2:n.1090+5G>C
XM_011528010.2:c.940+5G>C	XP_011526312.1:n.940+5G>C
XR_001753685.2:n.1057+5G>C
XR_001753686.2:n.1057+5G>C
NM_000527.5:c.940+5G>C MANE Select	NP_000518.1:n.940+5G>C
NM_001195798.2:c.940+5G>C	NP_001182727.1:n.940+5G>C
NM_001195799.2:c.817+5G>C	NP_001182728.1:n.817+5G>C
NM_001195800.2:c.436+5G>C	NP_001182729.1:n.436+5G>C
NM_001195803.2:c.559+5G>C	NP_001182732.1:n.559+5G>C