Canonical Allele Identifier: CA412177772

Gene: TUBGCP6

Linked Data

• gnomAD v4: 22-50220450-C-G
• MyVariant Identifiers: chr22:g.50658879C>G (hg19) ; chr22:g.50220450C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220450C>G , CM000684.2:g.50220450C>G	GRCh38
NC_000022.10:g.50658879C>G , CM000684.1:g.50658879C>G	GRCh37
NC_000022.9:g.49001006C>G	NCBI36
NG_032160.1:g.29522G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3909G>C MANE Select	ENSP00000248846.5:p.Gln1303His
ENST00000248846.9:c.3909G>C	ENSP00000248846.5:p.Gln1303His
ENST00000439308.6:c.3909G>C	ENSP00000397387.2:p.Gln1303His
ENST00000491449.5:n.2216G>C
ENST00000498611.5:n.3618-435G>C
NM_020461.3:c.3909G>C	NP_065194.2:p.Gln1303His
XR_938347.1:n.4474G>C
XR_938348.1:n.3050-435G>C
XR_001755343.2:n.4478G>C
XR_001755344.2:n.4478G>C
XR_002958720.1:n.3054-435G>C
XR_938347.2:n.4478G>C
NM_020461.4:c.3909G>C MANE Select	NP_065194.3:p.Gln1303His