Canonical Allele Identifier: CA1080647953
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753181881

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365844G>A , CM000667.2:g.118365844G>A GRCh38
NC_000005.9:g.117701539G>A , CM000667.1:g.117701539G>A GRCh37
NC_000005.8:g.117729438G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14337C>T