Canonical Allele Identifier: CA2045192347
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269285C= , CM000674.2:g.71269285C= GRCh38
NC_000012.11:g.71663065C= , CM000674.1:g.71663065C= GRCh37
NC_000012.10:g.69949332C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8066G= ENSP00000377003.2:n.-110+8066G=
ENST00000549421.1:n.206+13431G=