Canonical Allele Identifier: CA691537331
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71166082G>A , CM000674.2:g.71166082G>A GRCh38
NC_000012.11:g.71559862G>A , CM000674.1:g.71559862G>A GRCh37
NC_000012.10:g.69846129G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-109-8295C>T ENSP00000377003.2:n.-109-8295C>T
ENST00000549421.1:n.207-8295C>T