Canonical Allele Identifier: CA537645234
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1287372762
gnomAD v2: 2-170204862-C-T
gnomAD v3: 2-169348352-C-T
gnomAD v4: 2-169348352-C-T
MyVariant Identifiers: chr2:g.170204862C>T (hg19) chr2:g.169348352C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169348352C>T , CM000664.2:g.169348352C>T GRCh38
NC_000002.11:g.170204862C>T , CM000664.1:g.170204862C>T GRCh37
NC_000002.10:g.169913108C>T NCBI36
NG_012634.1:g.19261G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.79+13969G>A MANE Select ENSP00000496870.1:n.79+13969G>A
ENST00000263816.7:c.79+13969G>A ENSP00000263816.3:n.79+13969G>A
ENST00000443831.1:c.79+13969G>A ENSP00000409813.1:n.79+13969G>A
NM_004525.2:c.79+13969G>A NP_004516.2:n.79+13969G>A
XM_011511183.1:c.79+13969G>A XP_011509485.1:n.79+13969G>A
XM_011511185.1:c.79+13969G>A XP_011509487.1:n.79+13969G>A
NM_004525.3:c.79+13969G>A MANE Select NP_004516.2:n.79+13969G>A
XM_011511183.3:c.79+13969G>A XP_011509485.1:n.79+13969G>A
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