Canonical Allele Identifier: CA349152390
Gene: LRP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.170139480A>C (hg19) chr2:g.169282970A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169282970A>C , CM000664.2:g.169282970A>C GRCh38
NC_000002.11:g.170139480A>C , CM000664.1:g.170139480A>C GRCh37
NC_000002.10:g.169847726A>C NCBI36
NG_012634.1:g.84643T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.1074T>G MANE Select ENSP00000496870.1:p.Cys358Trp
ENST00000263816.7:c.1074T>G ENSP00000263816.3:p.Cys358Trp
ENST00000443831.1:c.1074T>G ENSP00000409813.1:p.Cys358Trp
NM_004525.2:c.1074T>G NP_004516.2:p.Cys358Trp
XM_011511183.1:c.1074T>G XP_011509485.1:p.Cys358Trp
XM_011511185.1:c.1074T>G XP_011509487.1:p.Cys358Trp
NM_004525.3:c.1074T>G MANE Select NP_004516.2:p.Cys358Trp
XM_011511183.3:c.1074T>G XP_011509485.1:p.Cys358Trp
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