Canonical Allele Identifier: CA679587748
Gene: LRP5 HGNC NCBI

Linked Data

dbSNP Id: rs1271455961
MyVariant Identifiers: chr11:g.68077295T>C (hg19) chr11:g.68309827T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68309827T>C , CM000673.2:g.68309827T>C GRCh38
NC_000011.9:g.68077295T>C , CM000673.1:g.68077295T>C GRCh37
NC_000011.8:g.67833871T>C NCBI36
NG_015835.1:g.2188T>C
NG_015835.2:g.2188T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011545029.1:c.118+10829T>C XP_011543331.1:n.118+10829T>C
XM_011545030.1:c.118+10829T>C XP_011543332.1:n.118+10829T>C
XM_011545031.1:c.118+10829T>C XP_011543333.1:n.118+10829T>C
XR_949925.1:n.133+10829T>C
XR_949926.1:n.133+10829T>C
XR_001747874.1:n.133+10829T>C
XR_949925.2:n.133+10829T>C
XR_949926.2:n.133+10829T>C
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