Canonical Allele Identifier: CA429920368
Gene: LRP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2832234
ClinVar RCV Id: RCV003689403
MyVariant Identifiers: chr2:g.170139387A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282877A>G , CM000664.2:g.169282877A>G GRCh38
NC_000002.11:g.170139387A>G , CM000664.1:g.170139387A>G GRCh37
NC_000002.10:g.169847633A>G NCBI36
NG_012634.1:g.84736T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.1167T>C MANE Select ENSP00000496870.1:p.Asp389=
ENST00000263816.7:c.1167T>C ENSP00000263816.3:p.Asp389=
ENST00000443831.1:c.1167T>C ENSP00000409813.1:p.Asp389=
NM_004525.2:c.1167T>C NP_004516.2:p.Asp389=
XM_011511183.1:c.1167T>C XP_011509485.1:p.Asp389=
XM_011511185.1:c.1167T>C XP_011509487.1:p.Asp389=
NM_004525.3:c.1167T>C MANE Select NP_004516.2:p.Asp389=
XM_011511183.3:c.1167T>C XP_011509485.1:p.Asp389=