Canonical Allele Identifier: CA703248169

Gene: LINC02323

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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