Canonical Allele Identifier: CA537972012
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1440615504
gnomAD v2: 2-170115753-T-G
gnomAD v3: 2-169259243-T-G
gnomAD v4: 2-169259243-T-G
MyVariant Identifiers: chr2:g.170115753T>G (hg19) chr2:g.169259243T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259243T>G , CM000664.2:g.169259243T>G GRCh38
NC_000002.11:g.170115753T>G , CM000664.1:g.170115753T>G GRCh37
NC_000002.10:g.169823999T>G NCBI36
NG_012634.1:g.108370A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2321-26A>C MANE Select ENSP00000496870.1:n.2321-26A>C
ENST00000263816.7:c.2321-26A>C ENSP00000263816.3:n.2321-26A>C
ENST00000443831.1:c.1910-26A>C ENSP00000409813.1:n.1910-26A>C
NM_004525.2:c.2321-26A>C NP_004516.2:n.2321-26A>C
XM_011511183.1:c.2321-26A>C XP_011509485.1:n.2321-26A>C
XM_011511184.1:c.32-26A>C XP_011509486.1:n.32-26A>C
XM_011511185.1:c.2321-26A>C XP_011509487.1:n.2321-26A>C
NM_004525.3:c.2321-26A>C MANE Select NP_004516.2:n.2321-26A>C
XM_011511183.3:c.2321-26A>C XP_011509485.1:n.2321-26A>C
XM_011511184.2:c.32-26A>C XP_011509486.1:n.32-26A>C
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