Canonical Allele Identifier: CA349158412

Gene: LRP2

Linked Data

• dbSNP Id: rs1437040751
• gnomAD v3: 2-169259127-T-C
• gnomAD v4: 2-169259127-T-C
• MyVariant Identifiers: chr2:g.170115637T>C (hg19) ; chr2:g.169259127T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259127T>C , CM000664.2:g.169259127T>C	GRCh38
NC_000002.11:g.170115637T>C , CM000664.1:g.170115637T>C	GRCh37
NC_000002.10:g.169823883T>C	NCBI36
NG_012634.1:g.108486A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.2411A>G MANE Select	ENSP00000496870.1:p.His804Arg
ENST00000263816.7:c.2411A>G	ENSP00000263816.3:p.His804Arg
ENST00000443831.1:c.2000A>G	ENSP00000409813.1:p.His667Arg
NM_004525.2:c.2411A>G	NP_004516.2:p.His804Arg
XM_011511183.1:c.2411A>G	XP_011509485.1:p.His804Arg
XM_011511184.1:c.122A>G	XP_011509486.1:p.His41Arg
XM_011511185.1:c.2411A>G	XP_011509487.1:p.His804Arg
NM_004525.3:c.2411A>G MANE Select	NP_004516.2:p.His804Arg
XM_011511183.3:c.2411A>G	XP_011509485.1:p.His804Arg
XM_011511184.2:c.122A>G	XP_011509486.1:p.His41Arg