Canonical Allele Identifier: CA412184072

Gene: TUBGCP6

Linked Data

• ClinVar Variation Id: 2081022
• ClinVar RCV Id: RCV002979609
• dbSNP Id: rs1182509162
• MyVariant Identifiers: chr22:g.50659535T>C (hg19) ; chr22:g.50221106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50221106T>C , CM000684.2:g.50221106T>C	GRCh38
NC_000022.10:g.50659535T>C , CM000684.1:g.50659535T>C	GRCh37
NC_000022.9:g.49001662T>C	NCBI36
NG_032160.1:g.28866A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3253A>G MANE Select	ENSP00000248846.5:p.Asn1085Asp
ENST00000248846.9:c.3253A>G	ENSP00000248846.5:p.Asn1085Asp
ENST00000439308.6:c.3253A>G	ENSP00000397387.2:p.Asn1085Asp
ENST00000491449.5:n.1560A>G
ENST00000498611.5:n.3617+169A>G
NM_020461.3:c.3253A>G	NP_065194.2:p.Asn1085Asp
XR_938347.1:n.3818A>G
XR_938348.1:n.3049+922A>G
XR_001755343.2:n.3822A>G
XR_001755344.2:n.3822A>G
XR_002958720.1:n.3053+922A>G
XR_938347.2:n.3822A>G
NM_020461.4:c.3253A>G MANE Select	NP_065194.3:p.Asn1085Asp