Canonical Allele Identifier: CA126242402

Gene: LINC02208

Linked Data

• dbSNP Id: rs1026698861
• MyVariant Identifiers: chr5:g.118365859C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365859C>A , CM000667.2:g.118365859C>A	GRCh38
NC_000005.9:g.117701554C>A , CM000667.1:g.117701554C>A	GRCh37
NC_000005.8:g.117729453C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14352G>T