Canonical Allele Identifier: CA900438610
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1271622461
MyVariant Identifiers: chr3:g.147935495T>C (hg19) chr3:g.148217708T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217708T>C , CM000665.2:g.148217708T>C GRCh38
NC_000003.11:g.147935495T>C , CM000665.1:g.147935495T>C GRCh37
NC_000003.10:g.149418185T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2802A>G
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