Canonical Allele Identifier: CA239502462

Gene: TSPAN8

Linked Data

• dbSNP Id: rs907459249
• gnomAD v3: 12-71269257-C-G
• gnomAD v4: 12-71269257-C-G
• MyVariant Identifiers: chr12:g.71663037C>G (hg19) ; chr12:g.71269257C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71269257C>G , CM000674.2:g.71269257C>G	GRCh38
NC_000012.11:g.71663037C>G , CM000674.1:g.71663037C>G	GRCh37
NC_000012.10:g.69949304C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393330.6:c.-110+8094G>C	ENSP00000377003.2:n.-110+8094G>C
ENST00000549421.1:n.206+13459G>C