Canonical Allele Identifier: CA515376726
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50659746C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221317C>G , CM000684.2:g.50221317C>G GRCh38
NC_000022.10:g.50659746C>G , CM000684.1:g.50659746C>G GRCh37
NC_000022.9:g.49001873C>G NCBI36
NG_032160.1:g.28655G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3042G>C MANE Select ENSP00000248846.5:p.Leu1014=
ENST00000248846.9:c.3042G>C ENSP00000248846.5:p.Leu1014=
ENST00000439308.6:c.3042G>C ENSP00000397387.2:p.Leu1014=
ENST00000491449.5:n.1349G>C
ENST00000498611.5:n.3575G>C
NM_020461.3:c.3042G>C NP_065194.2:p.Leu1014=
XR_938347.1:n.3607G>C
XR_938348.1:n.3049+711G>C
XR_001755343.2:n.3611G>C
XR_001755344.2:n.3611G>C
XR_002958720.1:n.3053+711G>C
XR_938347.2:n.3611G>C
NM_020461.4:c.3042G>C MANE Select NP_065194.3:p.Leu1014=