Canonical Allele Identifier: CA10308052
Gene: TUBGCP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 943680
ClinVar RCV Id: RCV001329147 RCV001213924
dbSNP Id: rs185642293
ExAC: 22:50659690 C / T
gnomAD v2: 22-50659690-C-T
gnomAD v3: 22-50221261-C-T
gnomAD v4: 22-50221261-C-T
MyVariant Identifiers: chr22:g.50659690C>T (hg19) chr22:g.50221261C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221261C>T , CM000684.2:g.50221261C>T GRCh38
NC_000022.10:g.50659690C>T , CM000684.1:g.50659690C>T GRCh37
NC_000022.9:g.49001817C>T NCBI36
NG_032160.1:g.28711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3098G>A MANE Select ENSP00000248846.5:p.Gly1033Asp
ENST00000248846.9:c.3098G>A ENSP00000248846.5:p.Gly1033Asp
ENST00000439308.6:c.3098G>A ENSP00000397387.2:p.Gly1033Asp
ENST00000491449.5:n.1405G>A
ENST00000498611.5:n.3617+14G>A
NM_020461.3:c.3098G>A NP_065194.2:p.Gly1033Asp
XR_938347.1:n.3663G>A
XR_938348.1:n.3049+767G>A
XR_001755343.2:n.3667G>A
XR_001755344.2:n.3667G>A
XR_002958720.1:n.3053+767G>A
XR_938347.2:n.3667G>A
NM_020461.4:c.3098G>A MANE Select NP_065194.3:p.Gly1033Asp
Search 100 bp 5'
Search 100 bp 3'