Canonical Allele Identifier: CA1306305455
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1558982499
gnomAD v4: 2-169154336-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154336G>T , CM000664.2:g.169154336G>T GRCh38
NC_000002.11:g.170010846G>T , CM000664.1:g.170010846G>T GRCh37
NC_000002.10:g.169719092G>T NCBI36
NG_012634.1:g.213277C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+124C>A MANE Select ENSP00000496870.1:n.12295+124C>A
ENST00000649153.1:c.3195+124C>A
ENST00000650252.1:c.1323+124C>A ENSP00000496887.1:n.1323+124C>A
ENST00000263816.7:c.12295+124C>A ENSP00000263816.3:n.12295+124C>A
NM_004525.2:c.12295+124C>A NP_004516.2:n.12295+124C>A
XM_011511183.1:c.12166+124C>A XP_011509485.1:n.12166+124C>A
XM_011511184.1:c.10006+124C>A XP_011509486.1:n.10006+124C>A
NM_004525.3:c.12295+124C>A MANE Select NP_004516.2:n.12295+124C>A
XM_011511183.3:c.12166+124C>A XP_011509485.1:n.12166+124C>A
XM_011511184.2:c.10006+124C>A XP_011509486.1:n.10006+124C>A
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