Canonical Allele Identifier: CA349152172
Gene: LRP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170139385G>T (hg19) chr2:g.169282875G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282875G>T , CM000664.2:g.169282875G>T GRCh38
NC_000002.11:g.170139385G>T , CM000664.1:g.170139385G>T GRCh37
NC_000002.10:g.169847631G>T NCBI36
NG_012634.1:g.84738C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.1169C>A MANE Select ENSP00000496870.1:p.Ser390Tyr
ENST00000263816.7:c.1169C>A ENSP00000263816.3:p.Ser390Tyr
ENST00000443831.1:c.1169C>A ENSP00000409813.1:p.Ser390Tyr
NM_004525.2:c.1169C>A NP_004516.2:p.Ser390Tyr
XM_011511183.1:c.1169C>A XP_011509485.1:p.Ser390Tyr
XM_011511185.1:c.1169C>A XP_011509487.1:p.Ser390Tyr
NM_004525.3:c.1169C>A MANE Select NP_004516.2:p.Ser390Tyr
XM_011511183.3:c.1169C>A XP_011509485.1:p.Ser390Tyr
Search 100 bp 5'
Search 100 bp 3'