Canonical Allele Identifier: CA2842409285
Gene: TSPAN8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269196T>C , CM000674.2:g.71269196T>C GRCh38
NC_000012.11:g.71662976T>C , CM000674.1:g.71662976T>C GRCh37
NC_000012.10:g.69949243T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-110+8155A>G ENSP00000377003.2:n.-110+8155A>G
ENST00000549421.1:n.206+13520A>G