Canonical Allele Identifier: CA760480320

Gene: LRP2

Linked Data

• dbSNP Id: rs1427121369
• gnomAD v3: 2-169259224-G-C
• gnomAD v4: 2-169259224-G-C
• MyVariant Identifiers: chr2:g.170115734G>C (hg19) ; chr2:g.169259224G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259224G>C , CM000664.2:g.169259224G>C	GRCh38
NC_000002.11:g.170115734G>C , CM000664.1:g.170115734G>C	GRCh37
NC_000002.10:g.169823980G>C	NCBI36
NG_012634.1:g.108389C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.2321-7C>G MANE Select	ENSP00000496870.1:n.2321-7C>G
ENST00000263816.7:c.2321-7C>G	ENSP00000263816.3:n.2321-7C>G
ENST00000443831.1:c.1910-7C>G	ENSP00000409813.1:n.1910-7C>G
NM_004525.2:c.2321-7C>G	NP_004516.2:n.2321-7C>G
XM_011511183.1:c.2321-7C>G	XP_011509485.1:n.2321-7C>G
XM_011511184.1:c.32-7C>G	XP_011509486.1:n.32-7C>G
XM_011511185.1:c.2321-7C>G	XP_011509487.1:n.2321-7C>G
NM_004525.3:c.2321-7C>G MANE Select	NP_004516.2:n.2321-7C>G
XM_011511183.3:c.2321-7C>G	XP_011509485.1:n.2321-7C>G
XM_011511184.2:c.32-7C>G	XP_011509486.1:n.32-7C>G