Canonical Allele Identifier: CA691674464

Gene: LINC02444

Linked Data

• dbSNP Id: rs11615274
• MyVariant Identifiers: chr12:g.73601132C>A (hg19) ; chr12:g.73207352C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.73207352C>A , CM000674.2:g.73207352C>A	GRCh38
NC_000012.11:g.73601132C>A , CM000674.1:g.73601132C>A	GRCh37
NC_000012.10:g.71887399C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110130.1:n.386-95C>A