Canonical Allele Identifier: CA691535046
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1193435461
gnomAD v3: 12-71269239-G-A
gnomAD v4: 12-71269239-G-A
MyVariant Identifiers: chr12:g.71663019G>A (hg19) chr12:g.71269239G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269239G>A , CM000674.2:g.71269239G>A GRCh38
NC_000012.11:g.71663019G>A , CM000674.1:g.71663019G>A GRCh37
NC_000012.10:g.69949286G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8112C>T ENSP00000377003.2:n.-110+8112C>T
ENST00000549421.1:n.206+13477C>T
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