Canonical Allele Identifier: CA2661813273
Gene: LRP2 HGNC NCBI

Linked Data

gnomAD v4: 2-169128972-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169128972A>G , CM000664.2:g.169128972A>G GRCh38
NC_000002.11:g.169985482A>G , CM000664.1:g.169985482A>G GRCh37
NC_000002.10:g.169693728A>G NCBI36
NG_012634.1:g.238641T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13800+41T>C MANE Select ENSP00000496870.1:n.13800+41T>C
ENST00000649153.1:c.4609+41T>C
ENST00000650252.1:c.2791+41T>C ENSP00000496887.1:n.2791+41T>C
ENST00000263816.7:c.13800+41T>C ENSP00000263816.3:n.13800+41T>C
NM_004525.2:c.13800+41T>C NP_004516.2:n.13800+41T>C
XM_011511183.1:c.13671+41T>C XP_011509485.1:n.13671+41T>C
XM_011511184.1:c.11511+41T>C XP_011509486.1:n.11511+41T>C
NM_004525.3:c.13800+41T>C MANE Select NP_004516.2:n.13800+41T>C
XM_011511183.3:c.13671+41T>C XP_011509485.1:n.13671+41T>C
XM_011511184.2:c.11511+41T>C XP_011509486.1:n.11511+41T>C
Search 100 bp 5'
Search 100 bp 3'