Canonical Allele Identifier: CA914507862

Gene: LRP2

Linked Data

• dbSNP Id: rs1559086559
• gnomAD v2: 2-170204793-T-C
• gnomAD v3: 2-169348283-T-C
• gnomAD v4: 2-169348283-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169348283T>C , CM000664.2:g.169348283T>C	GRCh38
NC_000002.11:g.170204793T>C , CM000664.1:g.170204793T>C	GRCh37
NC_000002.10:g.169913039T>C	NCBI36
NG_012634.1:g.19330A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.79+14038A>G MANE Select	ENSP00000496870.1:n.79+14038A>G
ENST00000263816.7:c.79+14038A>G	ENSP00000263816.3:n.79+14038A>G
ENST00000443831.1:c.79+14038A>G	ENSP00000409813.1:n.79+14038A>G
NM_004525.2:c.79+14038A>G	NP_004516.2:n.79+14038A>G
XM_011511183.1:c.79+14038A>G	XP_011509485.1:n.79+14038A>G
XM_011511185.1:c.79+14038A>G	XP_011509487.1:n.79+14038A>G
NM_004525.3:c.79+14038A>G MANE Select	NP_004516.2:n.79+14038A>G
XM_011511183.3:c.79+14038A>G	XP_011509485.1:n.79+14038A>G