Canonical Allele Identifier: CA185516651

Gene: LINC02964

Linked Data

• dbSNP Id: rs550239913
• gnomAD v2: 8-126539923-A-T
• gnomAD v3: 8-125527681-A-T
• gnomAD v4: 8-125527681-A-T
• MyVariant Identifiers: chr8:g.126539923A>T (hg19) ; chr8:g.125527681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125527681A>T , CM000670.2:g.125527681A>T	GRCh38
NC_000008.10:g.126539923A>T , CM000670.1:g.126539923A>T	GRCh37
NC_000008.9:g.126609105A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+54367A>T
XR_001746072.1:n.583+4668A>T
XR_001746073.1:n.583+4668A>T