Canonical Allele Identifier: CA2045192200
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269128G= , CM000674.2:g.71269128G= GRCh38
NC_000012.11:g.71662908G= , CM000674.1:g.71662908G= GRCh37
NC_000012.10:g.69949175G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-110+8223C= ENSP00000377003.2:n.-110+8223C=
ENST00000549421.1:n.206+13588C=