Canonical Allele Identifier: CA12322752
Gene: TBC1D22B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs149709

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37311157T>C , CM000668.2:g.37311157T>C GRCh38
NC_000006.11:g.37278933T>C , CM000668.1:g.37278933T>C GRCh37
NC_000006.10:g.37386911T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_017772.3:c.983-1761T>C VV NP_060242.2:p.=
NR_130108.1:n.1258-1761T>C
XM_011514738.1:c.983-1761T>C XP_011513040.1:p.=
XM_011514739.1:c.983-1761T>C XP_011513041.1:p.=
XR_241906.1:n.1034-1761T>C
XR_427833.1:n.1149-1723T>C
XR_926270.1:n.1149-1723T>C
XM_011514738.3:c.983-1761T>C XP_011513040.1:p.=
XM_011514739.2:c.983-1761T>C XP_011513041.1:p.=
XR_241906.2:n.1014-1761T>C
XR_427833.2:n.1129-1723T>C
XR_926270.3:n.1129-1723T>C
NM_017772.4:c.983-1761T>C VV MANE Preferred NP_060242.2:p.=
ENST00000373491.3:c.983-1761T>C ENSP00000362590.3:p.=