Canonical Allele Identifier: CA1955654
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs545496006
ExAC: 2:170139478 T / C
gnomAD v2: 2-170139478-T-C
gnomAD v3: 2-169282968-T-C
gnomAD v4: 2-169282968-T-C
MyVariant Identifiers: chr2:g.170139478T>C (hg19) chr2:g.169282968T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282968T>C , CM000664.2:g.169282968T>C GRCh38
NC_000002.11:g.170139478T>C , CM000664.1:g.170139478T>C GRCh37
NC_000002.10:g.169847724T>C NCBI36
NG_012634.1:g.84645A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.1076A>G MANE Select ENSP00000496870.1:p.Asp359Gly
ENST00000263816.7:c.1076A>G ENSP00000263816.3:p.Asp359Gly
ENST00000443831.1:c.1076A>G ENSP00000409813.1:p.Asp359Gly
NM_004525.2:c.1076A>G NP_004516.2:p.Asp359Gly
XM_011511183.1:c.1076A>G XP_011509485.1:p.Asp359Gly
XM_011511185.1:c.1076A>G XP_011509487.1:p.Asp359Gly
NM_004525.3:c.1076A>G MANE Select NP_004516.2:p.Asp359Gly
XM_011511183.3:c.1076A>G XP_011509485.1:p.Asp359Gly
Search 100 bp 5'
Search 100 bp 3'