Canonical Allele Identifier: CA260254682

Gene: LINC02302

Linked Data

• dbSNP Id: rs142332568
• gnomAD v2: 14-45106729-A-T
• gnomAD v3: 14-44637526-A-T
• gnomAD v4: 14-44637526-A-T
• MyVariant Identifiers: chr14:g.45106729A>T (hg19) ; chr14:g.44637526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44637526A>T , CM000676.2:g.44637526A>T	GRCh38
NC_000014.8:g.45106729A>T , CM000676.1:g.45106729A>T	GRCh37
NC_000014.7:g.44176479A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943800.1:n.226-40513T>A
XR_943801.1:n.226-40513T>A
XR_943806.1:n.226-40513T>A
XR_943808.1:n.126+160404T>A