Canonical Allele Identifier: CA412185201
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs2064519068

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221307T>C , CM000684.2:g.50221307T>C GRCh38
NC_000022.10:g.50659736T>C , CM000684.1:g.50659736T>C GRCh37
NC_000022.9:g.49001863T>C NCBI36
NG_032160.1:g.28665A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3052A>G MANE Select ENSP00000248846.5:p.Ser1018Gly
ENST00000248846.9:c.3052A>G ENSP00000248846.5:p.Ser1018Gly
ENST00000439308.6:c.3052A>G ENSP00000397387.2:p.Ser1018Gly
ENST00000491449.5:n.1359A>G
ENST00000498611.5:n.3585A>G
NM_020461.3:c.3052A>G NP_065194.2:p.Ser1018Gly
XR_938347.1:n.3617A>G
XR_938348.1:n.3049+721A>G
XR_001755343.2:n.3621A>G
XR_001755344.2:n.3621A>G
XR_002958720.1:n.3053+721A>G
XR_938347.2:n.3621A>G
NM_020461.4:c.3052A>G MANE Select NP_065194.3:p.Ser1018Gly