Canonical Allele Identifier: CA1621731052

Gene: TBC1D22B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311081T= , CM000668.2:g.37311081T=	GRCh38
NC_000006.11:g.37278857T= , CM000668.1:g.37278857T=	GRCh37
NC_000006.10:g.37386835T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373491.3:c.983-1837T= MANE Select	ENSP00000362590.3:n.983-1837T=
NM_017772.3:c.983-1837T=	NP_060242.2:n.983-1837T=
NR_130108.1:n.1258-1837T=
XM_011514738.1:c.983-1837T=	XP_011513040.1:n.983-1837T=
XM_011514739.1:c.983-1837T=	XP_011513041.1:n.983-1837T=
XR_241906.1:n.1034-1837T=
XR_427833.1:n.1149-1799T=
XR_926270.1:n.1149-1799T=
XM_011514738.3:c.983-1837T=	XP_011513040.1:n.983-1837T=
XM_011514739.2:c.983-1837T=	XP_011513041.1:n.983-1837T=
XR_241906.2:n.1014-1837T=
XR_427833.2:n.1129-1799T=
XR_926270.3:n.1129-1799T=
NM_017772.4:c.983-1837T= MANE Select	NP_060242.2:n.983-1837T=
NR_130108.2:n.1190-1837T=