Canonical Allele Identifier: CA2045192305
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1046286061

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269226G>A , CM000674.2:g.71269226G>A GRCh38
NC_000012.11:g.71663006G>A , CM000674.1:g.71663006G>A GRCh37
NC_000012.10:g.69949273G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8125C>T ENSP00000377003.2:n.-110+8125C>T
ENST00000549421.1:n.206+13490C>T