Canonical Allele Identifier: CA557432364

Gene: LINC02226

Linked Data

• dbSNP Id: rs1171635972
• gnomAD v2: 5-8439712-A-G
• gnomAD v3: 5-8439599-A-G
• gnomAD v4: 5-8439599-A-G
• MyVariant Identifiers: chr5:g.8439712A>G (hg19) ; chr5:g.8439599A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.8439599A>G , CM000667.2:g.8439599A>G	GRCh38
NC_000005.9:g.8439712A>G , CM000667.1:g.8439712A>G	GRCh37
NC_000005.8:g.8492712A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_039984.1:n.174+12624T>C