Canonical Allele Identifier: CA2045192334
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1849614949

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269261G>T , CM000674.2:g.71269261G>T GRCh38
NC_000012.11:g.71663041G>T , CM000674.1:g.71663041G>T GRCh37
NC_000012.10:g.69949308G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8090C>A ENSP00000377003.2:n.-110+8090C>A
ENST00000549421.1:n.206+13455C>A