Canonical Allele Identifier: CA378937214
Gene: TALDO1 HGNC NCBI

Linked Data

dbSNP Id: rs1863001576
gnomAD v3: 11-763865-C-A
gnomAD v4: 11-763865-C-A
MyVariant Identifiers: chr11:g.763865C>A (hg19) chr11:g.763865C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763865C>A , CM000673.2:g.763865C>A GRCh38
NC_000011.9:g.763865C>A , CM000673.1:g.763865C>A GRCh37
NC_000011.8:g.753865C>A NCBI36
NG_008160.1:g.21434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319006.8:c.756C>A MANE Select ENSP00000321259.3:p.Phe252Leu
ENST00000319006.7:c.756C>A ENSP00000321259.3:p.Phe252Leu
ENST00000528097.5:c.756C>A ENSP00000437098.1:p.Phe252Leu
NM_006755.1:c.756C>A NP_006746.1:p.Phe252Leu
NM_006755.2:c.756C>A MANE Select NP_006746.1:p.Phe252Leu
Search 100 bp 5'
Search 100 bp 3'