Canonical Allele Identifier: CA10308356

Gene: TUBGCP6

Linked Data

• ClinVar Variation Id: 2886224
• ClinVar RCV Id: RCV003719831
• dbSNP Id: rs760660473
• ExAC: 22:50662848 G / A
• gnomAD v2: 22-50662848-G-A
• gnomAD v4: 22-50224419-G-A
• MyVariant Identifiers: chr22:g.50662848G>A (hg19) ; chr22:g.50224419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50224419G>A , CM000684.2:g.50224419G>A	GRCh38
NC_000022.10:g.50662848G>A , CM000684.1:g.50662848G>A	GRCh37
NC_000022.9:g.49004975G>A	NCBI36
NG_032160.1:g.25553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.2067C>T MANE Select	ENSP00000248846.5:p.Asp689=
ENST00000248846.9:c.2067C>T	ENSP00000248846.5:p.Asp689=
ENST00000439308.6:c.2067C>T	ENSP00000397387.2:p.Asp689=
ENST00000473946.1:n.376C>T
ENST00000489511.5:n.84C>T
ENST00000491449.5:n.374C>T
ENST00000498611.5:n.2600C>T
NM_020461.3:c.2067C>T	NP_065194.2:p.Asp689=
XR_938347.1:n.2632C>T
XR_938348.1:n.2632C>T
XR_001755343.2:n.2636C>T
XR_001755344.2:n.2636C>T
XR_002958720.1:n.2636C>T
XR_938347.2:n.2636C>T
NM_020461.4:c.2067C>T MANE Select	NP_065194.3:p.Asp689=