Canonical Allele Identifier: CA412177899
Gene: TUBGCP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025113
ClinVar RCV Id: RCV001325390
dbSNP Id: rs909274169
gnomAD v2: 22-50658899-G-T
gnomAD v3: 22-50220470-G-T
gnomAD v4: 22-50220470-G-T
MyVariant Identifiers: chr22:g.50658899G>T (hg19) chr22:g.50220470G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220470G>T , CM000684.2:g.50220470G>T GRCh38
NC_000022.10:g.50658899G>T , CM000684.1:g.50658899G>T GRCh37
NC_000022.9:g.49001026G>T NCBI36
NG_032160.1:g.29502C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3889C>A MANE Select ENSP00000248846.5:p.Pro1297Thr
ENST00000248846.9:c.3889C>A ENSP00000248846.5:p.Pro1297Thr
ENST00000439308.6:c.3889C>A ENSP00000397387.2:p.Pro1297Thr
ENST00000491449.5:n.2196C>A
ENST00000498611.5:n.3618-455C>A
NM_020461.3:c.3889C>A NP_065194.2:p.Pro1297Thr
XR_938347.1:n.4454C>A
XR_938348.1:n.3050-455C>A
XR_001755343.2:n.4458C>A
XR_001755344.2:n.4458C>A
XR_002958720.1:n.3054-455C>A
XR_938347.2:n.4458C>A
NM_020461.4:c.3889C>A MANE Select NP_065194.3:p.Pro1297Thr
Search 100 bp 5'
Search 100 bp 3'