Canonical Allele Identifier: CA515376119
Gene: TUBGCP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081024
ClinVar RCV Id: RCV002979611
dbSNP Id: rs1303958353
gnomAD v3: 22-50221152-A-G
gnomAD v4: 22-50221152-A-G
MyVariant Identifiers: chr22:g.50659581A>G (hg19) chr22:g.50221152A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221152A>G , CM000684.2:g.50221152A>G GRCh38
NC_000022.10:g.50659581A>G , CM000684.1:g.50659581A>G GRCh37
NC_000022.9:g.49001708A>G NCBI36
NG_032160.1:g.28820T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3207T>C MANE Select ENSP00000248846.5:p.Asp1069=
ENST00000248846.9:c.3207T>C ENSP00000248846.5:p.Asp1069=
ENST00000439308.6:c.3207T>C ENSP00000397387.2:p.Asp1069=
ENST00000491449.5:n.1514T>C
ENST00000498611.5:n.3617+123T>C
NM_020461.3:c.3207T>C NP_065194.2:p.Asp1069=
XR_938347.1:n.3772T>C
XR_938348.1:n.3049+876T>C
XR_001755343.2:n.3776T>C
XR_001755344.2:n.3776T>C
XR_002958720.1:n.3053+876T>C
XR_938347.2:n.3776T>C
NM_020461.4:c.3207T>C MANE Select NP_065194.3:p.Asp1069=
Search 100 bp 5'
Search 100 bp 3'