Canonical Allele Identifier: CA2410732627
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs2064576532

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224508C>G , CM000684.2:g.50224508C>G GRCh38
NC_000022.10:g.50662937C>G , CM000684.1:g.50662937C>G GRCh37
NC_000022.9:g.49005064C>G NCBI36
NG_032160.1:g.25464G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248846.10:c.2065+3G>C MANE Select ENSP00000248846.5:n.2065+3G>C
ENST00000248846.9:c.2065+3G>C ENSP00000248846.5:n.2065+3G>C
ENST00000439308.6:c.2065+3G>C ENSP00000397387.2:n.2065+3G>C
ENST00000473946.1:n.374+3G>C
ENST00000489511.5:n.82+3G>C
ENST00000491449.5:n.372+3G>C
ENST00000498611.5:n.2598+3G>C
NM_020461.3:c.2065+3G>C NP_065194.2:n.2065+3G>C
XR_938347.1:n.2630+3G>C
XR_938348.1:n.2630+3G>C
XR_001755343.2:n.2634+3G>C
XR_001755344.2:n.2634+3G>C
XR_002958720.1:n.2634+3G>C
XR_938347.2:n.2634+3G>C
NM_020461.4:c.2065+3G>C MANE Select NP_065194.3:n.2065+3G>C