Canonical Allele Identifier: CA824368809

Gene: TBC1D22B

Linked Data

• dbSNP Id: rs1309832013
• gnomAD v3: 6-37311148-T-TTA
• gnomAD v4: 6-37311148-T-TTA
• MyVariant Identifiers: chr6:g.37278924_37278925insTA (hg19) ; chr6:g.37311148_37311149insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311156_37311157dup , CM000668.2:g.37311156_37311157dup	GRCh38
NC_000006.11:g.37278932_37278933dup , CM000668.1:g.37278932_37278933dup	GRCh37
NC_000006.10:g.37386910_37386911dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373491.3:c.983-1762_983-1761dup MANE Select	ENSP00000362590.3:n.983-1762_983-1761dup
NM_017772.3:c.983-1762_983-1761dup	NP_060242.2:n.983-1762_983-1761dup
NR_130108.1:n.1258-1762_1258-1761dup
XM_011514738.1:c.983-1762_983-1761dup	XP_011513040.1:n.983-1762_983-1761dup
XM_011514739.1:c.983-1762_983-1761dup	XP_011513041.1:n.983-1762_983-1761dup
XR_241906.1:n.1034-1762_1034-1761dup
XR_427833.1:n.1149-1724_1149-1723dup
XR_926270.1:n.1149-1724_1149-1723dup
XM_011514738.3:c.983-1762_983-1761dup	XP_011513040.1:n.983-1762_983-1761dup
XM_011514739.2:c.983-1762_983-1761dup	XP_011513041.1:n.983-1762_983-1761dup
XR_241906.2:n.1014-1762_1014-1761dup
XR_427833.2:n.1129-1724_1129-1723dup
XR_926270.3:n.1129-1724_1129-1723dup
NM_017772.4:c.983-1762_983-1761dup MANE Select	NP_060242.2:n.983-1762_983-1761dup
NR_130108.2:n.1190-1762_1190-1761dup