Canonical Allele Identifier: CA1955307
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs775830244

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259125A>G , CM000664.2:g.169259125A>G GRCh38
NC_000002.11:g.170115635A>G , CM000664.1:g.170115635A>G GRCh37
NC_000002.10:g.169823881A>G NCBI36
NG_012634.1:g.108488T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2413T>C MANE Select ENSP00000496870.1:p.Tyr805His
ENST00000263816.7:c.2413T>C ENSP00000263816.3:p.Tyr805His
ENST00000443831.1:c.2002T>C ENSP00000409813.1:p.Tyr668His
NM_004525.2:c.2413T>C NP_004516.2:p.Tyr805His
XM_011511183.1:c.2413T>C XP_011509485.1:p.Tyr805His
XM_011511184.1:c.124T>C XP_011509486.1:p.Tyr42His
XM_011511185.1:c.2413T>C XP_011509487.1:p.Tyr805His
NM_004525.3:c.2413T>C MANE Select NP_004516.2:p.Tyr805His
XM_011511183.3:c.2413T>C XP_011509485.1:p.Tyr805His
XM_011511184.2:c.124T>C XP_011509486.1:p.Tyr42His