Canonical Allele Identifier: CA349136972

Gene: LRP2

Linked Data

• dbSNP Id: rs2105358792
• MyVariant Identifiers: chr2:g.170010982C>G (hg19) ; chr2:g.169154472C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154472C>G , CM000664.2:g.169154472C>G	GRCh38
NC_000002.11:g.170010982C>G , CM000664.1:g.170010982C>G	GRCh37
NC_000002.10:g.169719228C>G	NCBI36
NG_012634.1:g.213141G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12283G>C MANE Select	ENSP00000496870.1:p.Asp4095His
ENST00000649153.1:c.3183G>C
ENST00000650252.1:c.1311G>C	ENSP00000496887.1:p.Arg437Ser
ENST00000263816.7:c.12283G>C	ENSP00000263816.3:p.Asp4095His
NM_004525.2:c.12283G>C	NP_004516.2:p.Asp4095His
XM_011511183.1:c.12154G>C	XP_011509485.1:p.Asp4052His
XM_011511184.1:c.9994G>C	XP_011509486.1:p.Asp3332His
NM_004525.3:c.12283G>C MANE Select	NP_004516.2:p.Asp4095His
XM_011511183.3:c.12154G>C	XP_011509485.1:p.Asp4052His
XM_011511184.2:c.9994G>C	XP_011509486.1:p.Asp3332His