Canonical Allele Identifier: CA429921087
Gene: LRP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170115639A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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