Canonical Allele Identifier: CA239502463
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs746862677
gnomAD v2: 12-71663039-T-C
gnomAD v3: 12-71269259-T-C
gnomAD v4: 12-71269259-T-C
MyVariant Identifiers: chr12:g.71663039T>C (hg19) chr12:g.71269259T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269259T>C , CM000674.2:g.71269259T>C GRCh38
NC_000012.11:g.71663039T>C , CM000674.1:g.71663039T>C GRCh37
NC_000012.10:g.69949306T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8092A>G ENSP00000377003.2:n.-110+8092A>G
ENST00000549421.1:n.206+13457A>G
Search 100 bp 5'
Search 100 bp 3'