Canonical Allele Identifier: CA239502483

Gene: TSPAN8

Linked Data

• dbSNP Id: rs191535350
• gnomAD v3: 12-71269401-C-T
• gnomAD v4: 12-71269401-C-T
• MyVariant Identifiers: chr12:g.71663181C>T (hg19) ; chr12:g.71269401C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71269401C>T , CM000674.2:g.71269401C>T	GRCh38
NC_000012.11:g.71663181C>T , CM000674.1:g.71663181C>T	GRCh37
NC_000012.10:g.69949448C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393330.6:c.-110+7950G>A	ENSP00000377003.2:n.-110+7950G>A
ENST00000549421.1:n.206+13315G>A