Canonical Allele Identifier: CA412185094
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs1450995823

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221291T>C , CM000684.2:g.50221291T>C GRCh38
NC_000022.10:g.50659720T>C , CM000684.1:g.50659720T>C GRCh37
NC_000022.9:g.49001847T>C NCBI36
NG_032160.1:g.28681A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3068A>G MANE Select ENSP00000248846.5:p.Glu1023Gly
ENST00000248846.9:c.3068A>G ENSP00000248846.5:p.Glu1023Gly
ENST00000439308.6:c.3068A>G ENSP00000397387.2:p.Glu1023Gly
ENST00000491449.5:n.1375A>G
ENST00000498611.5:n.3601A>G
NM_020461.3:c.3068A>G NP_065194.2:p.Glu1023Gly
XR_938347.1:n.3633A>G
XR_938348.1:n.3049+737A>G
XR_001755343.2:n.3637A>G
XR_001755344.2:n.3637A>G
XR_002958720.1:n.3053+737A>G
XR_938347.2:n.3637A>G
NM_020461.4:c.3068A>G MANE Select NP_065194.3:p.Glu1023Gly