Canonical Allele Identifier: CA1621731024
Gene: TBC1D22B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37311013T= , CM000668.2:g.37311013T= GRCh38
NC_000006.11:g.37278789T= , CM000668.1:g.37278789T= GRCh37
NC_000006.10:g.37386767T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373491.3:c.983-1905T= MANE Select ENSP00000362590.3:n.983-1905T=
NM_017772.3:c.983-1905T= NP_060242.2:n.983-1905T=
NR_130108.1:n.1258-1905T=
XM_011514738.1:c.983-1905T= XP_011513040.1:n.983-1905T=
XM_011514739.1:c.983-1905T= XP_011513041.1:n.983-1905T=
XR_241906.1:n.1034-1905T=
XR_427833.1:n.1149-1867T=
XR_926270.1:n.1149-1867T=
XM_011514738.3:c.983-1905T= XP_011513040.1:n.983-1905T=
XM_011514739.2:c.983-1905T= XP_011513041.1:n.983-1905T=
XR_241906.2:n.1014-1905T=
XR_427833.2:n.1129-1867T=
XR_926270.3:n.1129-1867T=
NM_017772.4:c.983-1905T= MANE Select NP_060242.2:n.983-1905T=
NR_130108.2:n.1190-1905T=