Canonical Allele Identifier: CA760475235

Gene: LRP2

Linked Data

• dbSNP Id: rs1343983908
• gnomAD v3: 2-169247707-T-A
• gnomAD v4: 2-169247707-T-A
• MyVariant Identifiers: chr2:g.170104217T>A (hg19) ; chr2:g.169247707T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247707T>A , CM000664.2:g.169247707T>A	GRCh38
NC_000002.11:g.170104217T>A , CM000664.1:g.170104217T>A	GRCh37
NC_000002.10:g.169812463T>A	NCBI36
NG_012634.1:g.119906A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2771-192A>T MANE Select	ENSP00000496870.1:n.2771-192A>T
ENST00000263816.7:c.2771-192A>T	ENSP00000263816.3:n.2771-192A>T
ENST00000443831.1:c.2360-192A>T	ENSP00000409813.1:n.2360-192A>T
NM_004525.2:c.2771-192A>T	NP_004516.2:n.2771-192A>T
XM_011511183.1:c.2771-192A>T	XP_011509485.1:n.2771-192A>T
XM_011511184.1:c.482-192A>T	XP_011509486.1:n.482-192A>T
XM_011511185.1:c.2771-192A>T	XP_011509487.1:n.2771-192A>T
NM_004525.3:c.2771-192A>T MANE Select	NP_004516.2:n.2771-192A>T
XM_011511183.3:c.2771-192A>T	XP_011509485.1:n.2771-192A>T
XM_011511184.2:c.482-192A>T	XP_011509486.1:n.482-192A>T