Canonical Allele Identifier: CA239502448

Gene: TSPAN8

Linked Data

• dbSNP Id: rs1051842023
• gnomAD v2: 12-71662933-G-A
• gnomAD v3: 12-71269153-G-A
• gnomAD v4: 12-71269153-G-A
• MyVariant Identifiers: chr12:g.71662933G>A (hg19) ; chr12:g.71269153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71269153G>A , CM000674.2:g.71269153G>A	GRCh38
NC_000012.11:g.71662933G>A , CM000674.1:g.71662933G>A	GRCh37
NC_000012.10:g.69949200G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393330.6:c.-110+8198C>T	ENSP00000377003.2:n.-110+8198C>T
ENST00000549421.1:n.206+13563C>T