Canonical Allele Identifier: CA23378619

Gene: LINC02778

Linked Data

• dbSNP Id: rs112285254
• gnomAD v2: 1-60651081-G-A
• gnomAD v3: 1-60185409-G-A
• gnomAD v4: 1-60185409-G-A
• MyVariant Identifiers: chr1:g.60651081G>A (hg19) ; chr1:g.60185409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.60185409G>A , CM000663.2:g.60185409G>A	GRCh38
NC_000001.10:g.60651081G>A , CM000663.1:g.60651081G>A	GRCh37
NC_000001.9:g.60423669G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947431.1:n.314-2308C>T
XR_947430.2:n.150-57416G>A
XR_947431.2:n.618-2308C>T