Canonical Allele Identifier: CA691535085

Gene: TSPAN8

Linked Data

• dbSNP Id: rs1305623140
• gnomAD v3: 12-71269295-A-G
• gnomAD v4: 12-71269295-A-G
• MyVariant Identifiers: chr12:g.71663075A>G (hg19) ; chr12:g.71269295A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71269295A>G , CM000674.2:g.71269295A>G	GRCh38
NC_000012.11:g.71663075A>G , CM000674.1:g.71663075A>G	GRCh37
NC_000012.10:g.69949342A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393330.6:c.-110+8056T>C	ENSP00000377003.2:n.-110+8056T>C
ENST00000549421.1:n.206+13421T>C