Canonical Allele Identifier: CA2700981159
Gene: LRP2 HGNC NCBI

Linked Data

dbSNP Id: rs2105571037
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169348374A>G , CM000664.2:g.169348374A>G GRCh38
NC_000002.11:g.170204884A>G , CM000664.1:g.170204884A>G GRCh37
NC_000002.10:g.169913130A>G NCBI36
NG_012634.1:g.19239T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.79+13947T>C MANE Select ENSP00000496870.1:n.79+13947T>C
ENST00000263816.7:c.79+13947T>C ENSP00000263816.3:n.79+13947T>C
ENST00000443831.1:c.79+13947T>C ENSP00000409813.1:n.79+13947T>C
NM_004525.2:c.79+13947T>C NP_004516.2:n.79+13947T>C
XM_011511183.1:c.79+13947T>C XP_011509485.1:n.79+13947T>C
XM_011511185.1:c.79+13947T>C XP_011509487.1:n.79+13947T>C
NM_004525.3:c.79+13947T>C MANE Select NP_004516.2:n.79+13947T>C
XM_011511183.3:c.79+13947T>C XP_011509485.1:n.79+13947T>C
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