Canonical Allele Identifier: CA15544149
Gene: TNKS HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.9555347T>C
GRCh37 chr8:g.9412857T>C
gnomAD v2:
8:9412857 T / C
gnomAD v3:
8:9555347 T / C
gnomAD v4:
chr8-9555347-T-C
Joint Max Group AF 0.40263645 (EAS)
Genomes Max Group AF 0.40263645 (EAS)
Exomes Max Group AF 0.10945252 (SAS)
dbSNP:
6990097
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9555347T>C , CM000670.2:g.9555347T>C GRCh38
NC_000008.10:g.9412857T>C , CM000670.1:g.9412857T>C GRCh37
NC_000008.9:g.9450267T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_006716263.2:c.-593T>C XP_006716326.1:n.-593T>C
XM_011543845.1:c.-593T>C XP_011542147.1:n.-593T>C
XM_011543846.1:c.-593T>C XP_011542148.1:n.-593T>C
XM_011543847.1:c.-593T>C XP_011542149.1:n.-593T>C
XM_006716263.4:c.-593T>C XP_006716326.1:n.-593T>C
XM_011543845.3:c.-593T>C XP_011542147.1:n.-593T>C
XM_011543846.3:c.-593T>C XP_011542148.1:n.-593T>C
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