Canonical Allele Identifier: CA680334706
Gene: TALDO1 HGNC NCBI

Linked Data

dbSNP Id: rs538249092
gnomAD v3: 11-763979-G-C
gnomAD v4: 11-763979-G-C
MyVariant Identifiers: chr11:g.763979G>C (hg19) chr11:g.763979G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763979G>C , CM000673.2:g.763979G>C GRCh38
NC_000011.9:g.763979G>C , CM000673.1:g.763979G>C GRCh37
NC_000011.8:g.753979G>C NCBI36
NG_008160.1:g.21548G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319006.8:c.835+35G>C MANE Select ENSP00000321259.3:n.835+35G>C
ENST00000319006.7:c.835+35G>C ENSP00000321259.3:n.835+35G>C
ENST00000528097.5:c.831+39G>C ENSP00000437098.1:n.831+39G>C
NM_006755.1:c.835+35G>C NP_006746.1:n.835+35G>C
NM_006755.2:c.835+35G>C MANE Select NP_006746.1:n.835+35G>C
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