Canonical Allele Identifier: CA1763972840

Gene: LINC00208

Linked Data

• dbSNP Id: rs1368177705

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577833T>A , CM000670.2:g.11577833T>A	GRCh38
NC_000008.10:g.11435342T>A , CM000670.1:g.11435342T>A	GRCh37
NC_000008.9:g.11472751T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.783+516T>A