Canonical Allele Identifier: CA515376365
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50659407G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220978G>T , CM000684.2:g.50220978G>T GRCh38
NC_000022.10:g.50659407G>T , CM000684.1:g.50659407G>T GRCh37
NC_000022.9:g.49001534G>T NCBI36
NG_032160.1:g.28994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3381C>A MANE Select ENSP00000248846.5:p.Thr1127=
ENST00000248846.9:c.3381C>A ENSP00000248846.5:p.Thr1127=
ENST00000439308.6:c.3381C>A ENSP00000397387.2:p.Thr1127=
ENST00000491449.5:n.1688C>A
ENST00000498611.5:n.3617+297C>A
NM_020461.3:c.3381C>A NP_065194.2:p.Thr1127=
XR_938347.1:n.3946C>A
XR_938348.1:n.3050-963C>A
XR_001755343.2:n.3950C>A
XR_001755344.2:n.3950C>A
XR_002958720.1:n.3054-963C>A
XR_938347.2:n.3950C>A
NM_020461.4:c.3381C>A MANE Select NP_065194.3:p.Thr1127=