Canonical Allele Identifier: CA691535056
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1259594673
gnomAD v3: 12-71269260-T-C
gnomAD v4: 12-71269260-T-C
MyVariant Identifiers: chr12:g.71663040T>C (hg19) chr12:g.71269260T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269260T>C , CM000674.2:g.71269260T>C GRCh38
NC_000012.11:g.71663040T>C , CM000674.1:g.71663040T>C GRCh37
NC_000012.10:g.69949307T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8091A>G ENSP00000377003.2:n.-110+8091A>G
ENST00000549421.1:n.206+13456A>G
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