Canonical Allele Identifier: CA949045354
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1868355864

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269242G>A , CM000674.2:g.71269242G>A GRCh38
NC_000012.11:g.71663022G>A , CM000674.1:g.71663022G>A GRCh37
NC_000012.10:g.69949289G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8109C>T ENSP00000377003.2:n.-110+8109C>T
ENST00000549421.1:n.206+13474C>T