Canonical Allele Identifier: CA1955653
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs767126588
ExAC: 2:170139477 G / T
gnomAD v2: 2-170139477-G-T
gnomAD v4: 2-169282967-G-T
MyVariant Identifiers: chr2:g.170139477G>T (hg19) chr2:g.169282967G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282967G>T , CM000664.2:g.169282967G>T GRCh38
NC_000002.11:g.170139477G>T , CM000664.1:g.170139477G>T GRCh37
NC_000002.10:g.169847723G>T NCBI36
NG_012634.1:g.84646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.1077C>A MANE Select ENSP00000496870.1:p.Asp359Glu
ENST00000263816.7:c.1077C>A ENSP00000263816.3:p.Asp359Glu
ENST00000443831.1:c.1077C>A ENSP00000409813.1:p.Asp359Glu
NM_004525.2:c.1077C>A NP_004516.2:p.Asp359Glu
XM_011511183.1:c.1077C>A XP_011509485.1:p.Asp359Glu
XM_011511185.1:c.1077C>A XP_011509487.1:p.Asp359Glu
NM_004525.3:c.1077C>A MANE Select NP_004516.2:p.Asp359Glu
XM_011511183.3:c.1077C>A XP_011509485.1:p.Asp359Glu
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