Canonical Allele Identifier: CA515376155
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50659353C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220924C>G , CM000684.2:g.50220924C>G GRCh38
NC_000022.10:g.50659353C>G , CM000684.1:g.50659353C>G GRCh37
NC_000022.9:g.49001480C>G NCBI36
NG_032160.1:g.29048G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3435G>C MANE Select ENSP00000248846.5:p.Gly1145=
ENST00000248846.9:c.3435G>C ENSP00000248846.5:p.Gly1145=
ENST00000439308.6:c.3435G>C ENSP00000397387.2:p.Gly1145=
ENST00000491449.5:n.1742G>C
ENST00000498611.5:n.3617+351G>C
NM_020461.3:c.3435G>C NP_065194.2:p.Gly1145=
XR_938347.1:n.4000G>C
XR_938348.1:n.3050-909G>C
XR_001755343.2:n.4004G>C
XR_001755344.2:n.4004G>C
XR_002958720.1:n.3054-909G>C
XR_938347.2:n.4004G>C
NM_020461.4:c.3435G>C MANE Select NP_065194.3:p.Gly1145=