Canonical Allele Identifier: CA2045192329
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269259T= , CM000674.2:g.71269259T= GRCh38
NC_000012.11:g.71663039T= , CM000674.1:g.71663039T= GRCh37
NC_000012.10:g.69949306T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8092A= ENSP00000377003.2:n.-110+8092A=
ENST00000549421.1:n.206+13457A=