Canonical Allele Identifier: CA814747149

Gene: LINC02226

Linked Data

• dbSNP Id: rs1290948304
• MyVariant Identifiers: chr5:g.8439735G>C (hg19) ; chr5:g.8439622G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.8439622G>C , CM000667.2:g.8439622G>C	GRCh38
NC_000005.9:g.8439735G>C , CM000667.1:g.8439735G>C	GRCh37
NC_000005.8:g.8492735G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_039984.1:n.174+12601C>G