Canonical Allele Identifier: CA584995101

Gene: LINC02964

Linked Data

• dbSNP Id: rs1388621589
• gnomAD v2: 8-126539964-A-C
• gnomAD v3: 8-125527722-A-C
• gnomAD v4: 8-125527722-A-C
• MyVariant Identifiers: chr8:g.126539964A>C (hg19) ; chr8:g.125527722A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125527722A>C , CM000670.2:g.125527722A>C	GRCh38
NC_000008.10:g.126539964A>C , CM000670.1:g.126539964A>C	GRCh37
NC_000008.9:g.126609146A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928628.1:n.256+54408A>C
XR_001746072.1:n.583+4709A>C
XR_001746073.1:n.583+4709A>C