Canonical Allele Identifier: CA2768090088
Gene: LINC02208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365700A>G , CM000667.2:g.118365700A>G GRCh38
NC_000005.9:g.117701395A>G , CM000667.1:g.117701395A>G GRCh37
NC_000005.8:g.117729294A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14193T>C