Canonical Allele Identifier: CA1576425893
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1561449421

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365845G>C , CM000667.2:g.118365845G>C GRCh38
NC_000005.9:g.117701540G>C , CM000667.1:g.117701540G>C GRCh37
NC_000005.8:g.117729439G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14338C>G