Canonical Allele Identifier: CA1306397486
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1685747496
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169348238C>A , CM000664.2:g.169348238C>A GRCh38
NC_000002.11:g.170204748C>A , CM000664.1:g.170204748C>A GRCh37
NC_000002.10:g.169912994C>A NCBI36
NG_012634.1:g.19375G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.79+14083G>T MANE Select ENSP00000496870.1:n.79+14083G>T
ENST00000263816.7:c.79+14083G>T ENSP00000263816.3:n.79+14083G>T
ENST00000443831.1:c.79+14083G>T ENSP00000409813.1:n.79+14083G>T
NM_004525.2:c.79+14083G>T NP_004516.2:n.79+14083G>T
XM_011511183.1:c.79+14083G>T XP_011509485.1:n.79+14083G>T
XM_011511185.1:c.79+14083G>T XP_011509487.1:n.79+14083G>T
NM_004525.3:c.79+14083G>T MANE Select NP_004516.2:n.79+14083G>T
XM_011511183.3:c.79+14083G>T XP_011509485.1:n.79+14083G>T
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