Canonical Allele Identifier: CA1621731082
Gene: TBC1D22B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37311182G= , CM000668.2:g.37311182G= GRCh38
NC_000006.11:g.37278958G= , CM000668.1:g.37278958G= GRCh37
NC_000006.10:g.37386936G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000373491.3:c.983-1736G= MANE Select ENSP00000362590.3:n.983-1736G=
NM_017772.3:c.983-1736G= NP_060242.2:n.983-1736G=
NR_130108.1:n.1258-1736G=
XM_011514738.1:c.983-1736G= XP_011513040.1:n.983-1736G=
XM_011514739.1:c.983-1736G= XP_011513041.1:n.983-1736G=
XR_241906.1:n.1034-1736G=
XR_427833.1:n.1149-1698G=
XR_926270.1:n.1149-1698G=
XM_011514738.3:c.983-1736G= XP_011513040.1:n.983-1736G=
XM_011514739.2:c.983-1736G= XP_011513041.1:n.983-1736G=
XR_241906.2:n.1014-1736G=
XR_427833.2:n.1129-1698G=
XR_926270.3:n.1129-1698G=
NM_017772.4:c.983-1736G= MANE Select NP_060242.2:n.983-1736G=
NR_130108.2:n.1190-1736G=