Canonical Allele Identifier: CA13950912

Gene: LINC02323

Linked Data

• dbSNP Id: rs11628318
• gnomAD v2: 14-103040087-T-A
• gnomAD v3: 14-102573750-T-A
• gnomAD v4: 14-102573750-T-A
• MyVariant Identifiers: chr14:g.103040087T>A (hg19) ; chr14:g.102573750T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102573750T>A , CM000676.2:g.102573750T>A	GRCh38
NC_000014.8:g.103040087T>A , CM000676.1:g.103040087T>A	GRCh37
NC_000014.7:g.102109840T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944240.1:n.609-6337T>A