Canonical Allele Identifier: CA349158661

Gene: LRP2

Linked Data

• dbSNP Id: rs1690435216
• MyVariant Identifiers: chr2:g.170115700A>C (hg19) ; chr2:g.169259190A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259190A>C , CM000664.2:g.169259190A>C	GRCh38
NC_000002.11:g.170115700A>C , CM000664.1:g.170115700A>C	GRCh37
NC_000002.10:g.169823946A>C	NCBI36
NG_012634.1:g.108423T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2348T>G MANE Select	ENSP00000496870.1:p.Val783Gly
ENST00000263816.7:c.2348T>G	ENSP00000263816.3:p.Val783Gly
ENST00000443831.1:c.1937T>G	ENSP00000409813.1:p.Val646Gly
NM_004525.2:c.2348T>G	NP_004516.2:p.Val783Gly
XM_011511183.1:c.2348T>G	XP_011509485.1:p.Val783Gly
XM_011511184.1:c.59T>G	XP_011509486.1:p.Val20Gly
XM_011511185.1:c.2348T>G	XP_011509487.1:p.Val783Gly
NM_004525.3:c.2348T>G MANE Select	NP_004516.2:p.Val783Gly
XM_011511183.3:c.2348T>G	XP_011509485.1:p.Val783Gly
XM_011511184.2:c.59T>G	XP_011509486.1:p.Val20Gly