Canonical Allele Identifier: CA605963534

Gene: TSPAN8

Linked Data

• dbSNP Id: rs1325358869
• gnomAD v2: 12-71663106-G-A
• gnomAD v3: 12-71269326-G-A
• gnomAD v4: 12-71269326-G-A
• MyVariant Identifiers: chr12:g.71663106G>A (hg19) ; chr12:g.71269326G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71269326G>A , CM000674.2:g.71269326G>A	GRCh38
NC_000012.11:g.71663106G>A , CM000674.1:g.71663106G>A	GRCh37
NC_000012.10:g.69949373G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393330.6:c.-110+8025C>T	ENSP00000377003.2:n.-110+8025C>T
ENST00000549421.1:n.206+13390C>T