Canonical Allele Identifier: CA480830057
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1868356670
gnomAD v3: 12-71269389-G-A
gnomAD v4: 12-71269389-G-A
MyVariant Identifiers: chr12:g.71663169G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269389G>A , CM000674.2:g.71269389G>A GRCh38
NC_000012.11:g.71663169G>A , CM000674.1:g.71663169G>A GRCh37
NC_000012.10:g.69949436G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-110+7962C>T ENSP00000377003.2:n.-110+7962C>T
ENST00000549421.1:n.206+13327C>T
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