Canonical Allele Identifier: CA2045192317
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269239G= , CM000674.2:g.71269239G= GRCh38
NC_000012.11:g.71663019G= , CM000674.1:g.71663019G= GRCh37
NC_000012.10:g.69949286G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8112C= ENSP00000377003.2:n.-110+8112C=
ENST00000549421.1:n.206+13477C=