Canonical Allele Identifier: CA706049070

Gene: LINC02302

Linked Data

• dbSNP Id: rs1412992867
• gnomAD v3: 14-44637481-T-C
• gnomAD v4: 14-44637481-T-C
• MyVariant Identifiers: chr14:g.45106684T>C (hg19) ; chr14:g.44637481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637481T>C , CM000676.2:g.44637481T>C	GRCh38
NC_000014.8:g.45106684T>C , CM000676.1:g.45106684T>C	GRCh37
NC_000014.7:g.44176434T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40468A>G
XR_943801.1:n.226-40468A>G
XR_943806.1:n.226-40468A>G
XR_943808.1:n.126+160449A>G