Canonical Allele Identifier: CA260254663

Gene: LINC02302

Linked Data

• dbSNP Id: rs1012086163
• gnomAD v3: 14-44637388-C-A
• gnomAD v4: 14-44637388-C-A
• MyVariant Identifiers: chr14:g.45106591C>A (hg19) ; chr14:g.44637388C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637388C>A , CM000676.2:g.44637388C>A	GRCh38
NC_000014.8:g.45106591C>A , CM000676.1:g.45106591C>A	GRCh37
NC_000014.7:g.44176341C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40375G>T
XR_943801.1:n.226-40375G>T
XR_943806.1:n.226-40375G>T
XR_943808.1:n.126+160542G>T