Canonical Allele Identifier: CA846003711

Gene: LINC00208

Linked Data

• dbSNP Id: rs1248500781
• MyVariant Identifiers: chr8:g.11435449T>C (hg19) ; chr8:g.11577940T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577940T>C , CM000670.2:g.11577940T>C	GRCh38
NC_000008.10:g.11435449T>C , CM000670.1:g.11435449T>C	GRCh37
NC_000008.9:g.11472858T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-430T>C