Canonical Allele Identifier: CA557432355

Gene: LINC02226

Linked Data

• dbSNP Id: rs1347331661
• gnomAD v2: 5-8439588-C-CA
• gnomAD v3: 5-8439475-C-CA
• gnomAD v4: 5-8439475-C-CA
• MyVariant Identifiers: chr5:g.8439588_8439589insA (hg19) ; chr5:g.8439475_8439476insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.8439482dup , CM000667.2:g.8439482dup	GRCh38
NC_000005.9:g.8439595dup , CM000667.1:g.8439595dup	GRCh37
NC_000005.8:g.8492595dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_039984.1:n.174+12747dup