Canonical Allele Identifier: CA949045331
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1592391704
gnomAD v3: 12-71269185-C-T
gnomAD v4: 12-71269185-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71269185C>T , CM000674.2:g.71269185C>T GRCh38
NC_000012.11:g.71662965C>T , CM000674.1:g.71662965C>T GRCh37
NC_000012.10:g.69949232C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393330.6:c.-110+8166G>A ENSP00000377003.2:n.-110+8166G>A
ENST00000549421.1:n.206+13531G>A
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