Canonical Allele Identifier: CA824368778

Gene: TBC1D22B

Linked Data

• dbSNP Id: rs1373253927
• gnomAD v3: 6-37311028-T-A
• gnomAD v4: 6-37311028-T-A
• MyVariant Identifiers: chr6:g.37278804T>A (hg19) ; chr6:g.37311028T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311028T>A , CM000668.2:g.37311028T>A	GRCh38
NC_000006.11:g.37278804T>A , CM000668.1:g.37278804T>A	GRCh37
NC_000006.10:g.37386782T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373491.3:c.983-1890T>A MANE Select	ENSP00000362590.3:n.983-1890T>A
NM_017772.3:c.983-1890T>A	NP_060242.2:n.983-1890T>A
NR_130108.1:n.1258-1890T>A
XM_011514738.1:c.983-1890T>A	XP_011513040.1:n.983-1890T>A
XM_011514739.1:c.983-1890T>A	XP_011513041.1:n.983-1890T>A
XR_241906.1:n.1034-1890T>A
XR_427833.1:n.1149-1852T>A
XR_926270.1:n.1149-1852T>A
XM_011514738.3:c.983-1890T>A	XP_011513040.1:n.983-1890T>A
XM_011514739.2:c.983-1890T>A	XP_011513041.1:n.983-1890T>A
XR_241906.2:n.1014-1890T>A
XR_427833.2:n.1129-1852T>A
XR_926270.3:n.1129-1852T>A
NM_017772.4:c.983-1890T>A MANE Select	NP_060242.2:n.983-1890T>A
NR_130108.2:n.1190-1890T>A