Canonical Allele Identifier: CA1576425904
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753182254

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365863_118365864insAATTCT , CM000667.2:g.118365863_118365864insAATTCT GRCh38
NC_000005.9:g.117701558_117701559insAATTCT , CM000667.1:g.117701558_117701559insAATTCT GRCh37
NC_000005.8:g.117729457_117729458insAATTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14357_2658-14356insAGAATT