Canonical Allele Identifier: CA59898021

Gene: LRP2

Linked Data

• dbSNP Id: rs576088875
• gnomAD v4: 2-169154419-G-A
• MyVariant Identifiers: chr2:g.170010929G>A (hg19) ; chr2:g.169154419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154419G>A , CM000664.2:g.169154419G>A	GRCh38
NC_000002.11:g.170010929G>A , CM000664.1:g.170010929G>A	GRCh37
NC_000002.10:g.169719175G>A	NCBI36
NG_012634.1:g.213194C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12295+41C>T MANE Select	ENSP00000496870.1:n.12295+41C>T
ENST00000649153.1:c.3195+41C>T
ENST00000650252.1:c.1323+41C>T	ENSP00000496887.1:n.1323+41C>T
ENST00000263816.7:c.12295+41C>T	ENSP00000263816.3:n.12295+41C>T
NM_004525.2:c.12295+41C>T	NP_004516.2:n.12295+41C>T
XM_011511183.1:c.12166+41C>T	XP_011509485.1:n.12166+41C>T
XM_011511184.1:c.10006+41C>T	XP_011509486.1:n.10006+41C>T
NM_004525.3:c.12295+41C>T MANE Select	NP_004516.2:n.12295+41C>T
XM_011511183.3:c.12166+41C>T	XP_011509485.1:n.12166+41C>T
XM_011511184.2:c.10006+41C>T	XP_011509486.1:n.10006+41C>T