Canonical Allele Identifier: CA626836738
Gene: TACO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109775
ClinVar RCV Id: RCV003042043
dbSNP Id: rs747730142
gnomAD v2: 17-61683661-T-C
gnomAD v4: 17-63606301-T-C
MyVariant Identifiers: chr17:g.61683661T>C (hg19) chr17:g.63606301T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63606301T>C , CM000679.2:g.63606301T>C GRCh38
NC_000017.10:g.61683661T>C , CM000679.1:g.61683661T>C GRCh37
NC_000017.9:g.59037393T>C NCBI36
NG_016979.1:g.10431T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682060.1:n.150-12T>C
ENST00000684587.1:c.385-12T>C ENSP00000507435.1:n.385-12T>C
ENST00000690765.1:c.*214-12T>C ENSP00000510085.1:n.*214-12T>C
ENST00000258975.7:c.388-12T>C MANE Select ENSP00000258975.6:n.388-12T>C
ENST00000258975.6:c.388-12T>C ENSP00000258975.6:n.388-12T>C
ENST00000581120.1:n.590-12T>C
NM_016360.3:c.388-12T>C NP_057444.2:n.388-12T>C
NM_016360.4:c.388-12T>C MANE Select NP_057444.2:n.388-12T>C
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