Canonical Allele Identifier: CA412103182
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs1601589848

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224405T>C , CM000684.2:g.50224405T>C GRCh38
NC_000022.10:g.50662834T>C , CM000684.1:g.50662834T>C GRCh37
NC_000022.9:g.49004961T>C NCBI36
NG_032160.1:g.25567A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.2081A>G MANE Select ENSP00000248846.5:p.Glu694Gly
ENST00000248846.9:c.2081A>G ENSP00000248846.5:p.Glu694Gly
ENST00000439308.6:c.2081A>G ENSP00000397387.2:p.Glu694Gly
ENST00000473946.1:n.390A>G
ENST00000489511.5:n.98A>G
ENST00000491449.5:n.388A>G
ENST00000498611.5:n.2614A>G
NM_020461.3:c.2081A>G NP_065194.2:p.Glu694Gly
XR_938347.1:n.2646A>G
XR_938348.1:n.2646A>G
XR_001755343.2:n.2650A>G
XR_001755344.2:n.2650A>G
XR_002958720.1:n.2650A>G
XR_938347.2:n.2650A>G
NM_020461.4:c.2081A>G MANE Select NP_065194.3:p.Glu694Gly