Canonical Allele Identifier: CA239502459
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1046286061
gnomAD v2: 12-71663006-G-C
gnomAD v3: 12-71269226-G-C
gnomAD v4: 12-71269226-G-C
MyVariant Identifiers: chr12:g.71663006G>C (hg19) chr12:g.71269226G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269226G>C , CM000674.2:g.71269226G>C GRCh38
NC_000012.11:g.71663006G>C , CM000674.1:g.71663006G>C GRCh37
NC_000012.10:g.69949273G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393330.6:c.-110+8125C>G ENSP00000377003.2:n.-110+8125C>G
ENST00000549421.1:n.206+13490C>G
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