Canonical Allele Identifier: CA824368785

Gene: TBC1D22B

Linked Data

• dbSNP Id: rs1452205668
• MyVariant Identifiers: chr6:g.37278816C>T (hg19) ; chr6:g.37311040C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311040C>T , CM000668.2:g.37311040C>T	GRCh38
NC_000006.11:g.37278816C>T , CM000668.1:g.37278816C>T	GRCh37
NC_000006.10:g.37386794C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373491.3:c.983-1878C>T MANE Select	ENSP00000362590.3:n.983-1878C>T
NM_017772.3:c.983-1878C>T	NP_060242.2:n.983-1878C>T
NR_130108.1:n.1258-1878C>T
XM_011514738.1:c.983-1878C>T	XP_011513040.1:n.983-1878C>T
XM_011514739.1:c.983-1878C>T	XP_011513041.1:n.983-1878C>T
XR_241906.1:n.1034-1878C>T
XR_427833.1:n.1149-1840C>T
XR_926270.1:n.1149-1840C>T
XM_011514738.3:c.983-1878C>T	XP_011513040.1:n.983-1878C>T
XM_011514739.2:c.983-1878C>T	XP_011513041.1:n.983-1878C>T
XR_241906.2:n.1014-1878C>T
XR_427833.2:n.1129-1840C>T
XR_926270.3:n.1129-1840C>T
NM_017772.4:c.983-1878C>T MANE Select	NP_060242.2:n.983-1878C>T
NR_130108.2:n.1190-1878C>T