Canonical Allele Identifier: CA1306349736
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1422093292
gnomAD v4: 2-169247578-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247578G>C , CM000664.2:g.169247578G>C GRCh38
NC_000002.11:g.170104088G>C , CM000664.1:g.170104088G>C GRCh37
NC_000002.10:g.169812334G>C NCBI36
NG_012634.1:g.120035C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2771-63C>G MANE Select ENSP00000496870.1:n.2771-63C>G
ENST00000263816.7:c.2771-63C>G ENSP00000263816.3:n.2771-63C>G
ENST00000443831.1:c.2360-63C>G ENSP00000409813.1:n.2360-63C>G
NM_004525.2:c.2771-63C>G NP_004516.2:n.2771-63C>G
XM_011511183.1:c.2771-63C>G XP_011509485.1:n.2771-63C>G
XM_011511184.1:c.482-63C>G XP_011509486.1:n.482-63C>G
XM_011511185.1:c.2771-63C>G XP_011509487.1:n.2771-63C>G
NM_004525.3:c.2771-63C>G MANE Select NP_004516.2:n.2771-63C>G
XM_011511183.3:c.2771-63C>G XP_011509485.1:n.2771-63C>G
XM_011511184.2:c.482-63C>G XP_011509486.1:n.482-63C>G
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