Canonical Allele Identifier: CA754042276

Gene: TUBGCP6

Linked Data

• dbSNP Id: rs1343584135
• gnomAD v3: 22-50224472-C-T
• gnomAD v4: 22-50224472-C-T
• MyVariant Identifiers: chr22:g.50662901C>T (hg19) ; chr22:g.50224472C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50224472C>T , CM000684.2:g.50224472C>T	GRCh38
NC_000022.10:g.50662901C>T , CM000684.1:g.50662901C>T	GRCh37
NC_000022.9:g.49005028C>T	NCBI36
NG_032160.1:g.25500G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.2065+39G>A MANE Select	ENSP00000248846.5:n.2065+39G>A
ENST00000248846.9:c.2065+39G>A	ENSP00000248846.5:n.2065+39G>A
ENST00000439308.6:c.2065+39G>A	ENSP00000397387.2:n.2065+39G>A
ENST00000473946.1:n.374+39G>A
ENST00000489511.5:n.82+39G>A
ENST00000491449.5:n.372+39G>A
ENST00000498611.5:n.2598+39G>A
NM_020461.3:c.2065+39G>A	NP_065194.2:n.2065+39G>A
XR_938347.1:n.2630+39G>A
XR_938348.1:n.2630+39G>A
XR_001755343.2:n.2634+39G>A
XR_001755344.2:n.2634+39G>A
XR_002958720.1:n.2634+39G>A
XR_938347.2:n.2634+39G>A
NM_020461.4:c.2065+39G>A MANE Select	NP_065194.3:n.2065+39G>A