Canonical Allele Identifier: CA1576425834
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1261105894

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365740C>A , CM000667.2:g.118365740C>A GRCh38
NC_000005.9:g.117701435C>A , CM000667.1:g.117701435C>A GRCh37
NC_000005.8:g.117729334C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14233G>T