Canonical Allele Identifier: CA113946407

Gene: LINC02226

Linked Data

• dbSNP Id: rs12187557
• gnomAD v2: 5-8439670-T-C
• gnomAD v3: 5-8439557-T-C
• gnomAD v4: 5-8439557-T-C
• MyVariant Identifiers: chr5:g.8439670T>C (hg19) ; chr5:g.8439557T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.8439557T>C , CM000667.2:g.8439557T>C	GRCh38
NC_000005.9:g.8439670T>C , CM000667.1:g.8439670T>C	GRCh37
NC_000005.8:g.8492670T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_039984.1:n.174+12666A>G