Canonical Allele Identifier: CA2045182352
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71183321G>A , CM000674.2:g.71183321G>A GRCh38
NC_000012.11:g.71577101G>A , CM000674.1:g.71577101G>A GRCh37
NC_000012.10:g.69863368G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-109-25534C>T ENSP00000377003.2:n.-109-25534C>T
ENST00000549421.1:n.207-25534C>T