Canonical Allele Identifier: CA2045192315
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1947153935

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269237A>G , CM000674.2:g.71269237A>G GRCh38
NC_000012.11:g.71663017A>G , CM000674.1:g.71663017A>G GRCh37
NC_000012.10:g.69949284A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8114T>C ENSP00000377003.2:n.-110+8114T>C
ENST00000549421.1:n.206+13479T>C