Canonical Allele Identifier: CA2045192438
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1384008699

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269408C>T , CM000674.2:g.71269408C>T GRCh38
NC_000012.11:g.71663188C>T , CM000674.1:g.71663188C>T GRCh37
NC_000012.10:g.69949455C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-110+7943G>A ENSP00000377003.2:n.-110+7943G>A
ENST00000549421.1:n.206+13308G>A