Canonical Allele Identifier: CA760469629
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs1479999121

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154392A>G , CM000664.2:g.169154392A>G GRCh38
NC_000002.11:g.170010902A>G , CM000664.1:g.170010902A>G GRCh37
NC_000002.10:g.169719148A>G NCBI36
NG_012634.1:g.213221T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+68T>C MANE Select ENSP00000496870.1:n.12295+68T>C
ENST00000649153.1:c.3195+68T>C
ENST00000650252.1:c.1323+68T>C ENSP00000496887.1:n.1323+68T>C
ENST00000263816.7:c.12295+68T>C ENSP00000263816.3:n.12295+68T>C
NM_004525.2:c.12295+68T>C NP_004516.2:n.12295+68T>C
XM_011511183.1:c.12166+68T>C XP_011509485.1:n.12166+68T>C
XM_011511184.1:c.10006+68T>C XP_011509486.1:n.10006+68T>C
NM_004525.3:c.12295+68T>C MANE Select NP_004516.2:n.12295+68T>C
XM_011511183.3:c.12166+68T>C XP_011509485.1:n.12166+68T>C
XM_011511184.2:c.10006+68T>C XP_011509486.1:n.10006+68T>C