Canonical Allele Identifier: CA1576425855
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1198928475

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365783A>T , CM000667.2:g.118365783A>T GRCh38
NC_000005.9:g.117701478A>T , CM000667.1:g.117701478A>T GRCh37
NC_000005.8:g.117729377A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14276T>A