Canonical Allele Identifier: CA59921096
Gene: LRP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 893656
dbSNP Id: rs544785940

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259129A>C , CM000664.2:g.169259129A>C GRCh38
NC_000002.11:g.170115639A>C , CM000664.1:g.170115639A>C GRCh37
NC_000002.10:g.169823885A>C NCBI36
NG_012634.1:g.108484T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2409T>G MANE Select ENSP00000496870.1:p.Ser803=
ENST00000263816.7:c.2409T>G ENSP00000263816.3:p.Ser803=
ENST00000443831.1:c.1998T>G ENSP00000409813.1:p.Ser666=
NM_004525.2:c.2409T>G NP_004516.2:p.Ser803=
XM_011511183.1:c.2409T>G XP_011509485.1:p.Ser803=
XM_011511184.1:c.120T>G XP_011509486.1:p.Ser40=
XM_011511185.1:c.2409T>G XP_011509487.1:p.Ser803=
NM_004525.3:c.2409T>G MANE Select NP_004516.2:p.Ser803=
XM_011511183.3:c.2409T>G XP_011509485.1:p.Ser803=
XM_011511184.2:c.120T>G XP_011509486.1:p.Ser40=