Canonical Allele Identifier: CA10307936
Gene: TUBGCP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089141
ClinVar RCV Id: RCV003018277
dbSNP Id: rs771759610
ExAC: 22:50659312 T / A
gnomAD v2: 22-50659312-T-A
gnomAD v3: 22-50220883-T-A
gnomAD v4: 22-50220883-T-A
MyVariant Identifiers: chr22:g.50659312T>A (hg19) chr22:g.50220883T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220883T>A , CM000684.2:g.50220883T>A GRCh38
NC_000022.10:g.50659312T>A , CM000684.1:g.50659312T>A GRCh37
NC_000022.9:g.49001439T>A NCBI36
NG_032160.1:g.29089A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3476A>T MANE Select ENSP00000248846.5:p.Asn1159Ile
ENST00000248846.9:c.3476A>T ENSP00000248846.5:p.Asn1159Ile
ENST00000439308.6:c.3476A>T ENSP00000397387.2:p.Asn1159Ile
ENST00000491449.5:n.1783A>T
ENST00000498611.5:n.3617+392A>T
NM_020461.3:c.3476A>T NP_065194.2:p.Asn1159Ile
XR_938347.1:n.4041A>T
XR_938348.1:n.3050-868A>T
XR_001755343.2:n.4045A>T
XR_001755344.2:n.4045A>T
XR_002958720.1:n.3054-868A>T
XR_938347.2:n.4045A>T
NM_020461.4:c.3476A>T MANE Select NP_065194.3:p.Asn1159Ile
Search 100 bp 5'
Search 100 bp 3'