Canonical Allele Identifier: CA1621731017

Gene: TBC1D22B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37310993G= , CM000668.2:g.37310993G=	GRCh38
NC_000006.11:g.37278769G= , CM000668.1:g.37278769G=	GRCh37
NC_000006.10:g.37386747G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373491.3:c.983-1925G= MANE Select	ENSP00000362590.3:n.983-1925G=
NM_017772.3:c.983-1925G=	NP_060242.2:n.983-1925G=
NR_130108.1:n.1258-1925G=
XM_011514738.1:c.983-1925G=	XP_011513040.1:n.983-1925G=
XM_011514739.1:c.983-1925G=	XP_011513041.1:n.983-1925G=
XR_241906.1:n.1034-1925G=
XR_427833.1:n.1149-1887G=
XR_926270.1:n.1149-1887G=
XM_011514738.3:c.983-1925G=	XP_011513040.1:n.983-1925G=
XM_011514739.2:c.983-1925G=	XP_011513041.1:n.983-1925G=
XR_241906.2:n.1014-1925G=
XR_427833.2:n.1129-1887G=
XR_926270.3:n.1129-1887G=
NM_017772.4:c.983-1925G= MANE Select	NP_060242.2:n.983-1925G=
NR_130108.2:n.1190-1925G=