Canonical Allele Identifier: CA1409673964
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1712870228
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217711A>G , CM000665.2:g.148217711A>G GRCh38
NC_000003.11:g.147935498A>G , CM000665.1:g.147935498A>G GRCh37
NC_000003.10:g.149418188A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2799T>C
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