Canonical Allele Identifier: CA571907181

Gene: ARID1B

Linked Data

• dbSNP Id: rs1217146091
• gnomAD v2: 6-157099732-C-CG
• gnomAD v3: 6-156778598-C-CG
• gnomAD v4: 6-156778598-C-CG
• MyVariant Identifiers: chr6:g.157099732_157099733insG (hg19) ; chr6:g.156778598_156778599insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778598_156778599insG , CM000668.2:g.156778598_156778599insG	GRCh38
NC_000006.11:g.157099732_157099733insG , CM000668.1:g.157099732_157099733insG	GRCh37
NC_000006.10:g.157141424_157141425insG	NCBI36
NG_032093.1:g.5669_5670insG
NG_032093.2:g.5669_5670insG
NG_066624.1:g.7573_7574insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.918_919insG	ENSP00000055163.8:p.Pro307AlafsTer8
ENST00000414678.8:c.918_919insG	ENSP00000412835.3:p.Pro307AlafsTer8
ENST00000637015.2:c.918_919insG	ENSP00000489729.2:p.Pro307AlafsTer8
ENST00000346085.10:c.918_919insG	ENSP00000344546.5:p.Pro307AlafsTer8
ENST00000350026.10:c.669_670insG	ENSP00000055163.7:p.Pro224AlafsTer8
ENST00000636930.2:c.918_919insG MANE Select	ENSP00000490491.2:p.Pro307AlafsTer8
ENST00000647938.1:c.669_670insG	ENSP00000498155.1:p.Pro224AlafsTer8
ENST00000674298.1:c.658_659insG
ENST00000346085.9:c.669_670insG	ENSP00000344546.4:p.Pro224AlafsTer8
ENST00000350026.9:c.669_670insG	ENSP00000055163.7:p.Pro224AlafsTer8
NM_017519.2:c.669_670insG	NP_059989.2:p.Pro224AlafsTer8
NM_020732.3:c.669_670insG	NP_065783.3:p.Pro224AlafsTer8
XM_005267069.3:c.669_670insG	XP_005267126.2:p.Pro224AlafsTer8
NM_001346813.1:c.669_670insG	NP_001333742.1:p.Pro224AlafsTer8
XM_011535984.2:c.669_670insG	XP_011534286.2:p.Pro224AlafsTer8
XM_017011103.2:c.669_670insG	XP_016866592.1:p.Pro224AlafsTer8
XM_017011104.1:c.669_670insG	XP_016866593.1:p.Pro224AlafsTer8
XM_017011105.2:c.669_670insG	XP_016866594.1:p.Pro224AlafsTer8
XM_017011106.2:c.669_670insG	XP_016866595.1:p.Pro224AlafsTer8
XM_017011107.2:c.669_670insG	XP_016866596.1:p.Pro224AlafsTer8
XR_002956289.1:n.752_753insG
NM_001371656.1:c.918_919insG	NP_001358585.1:p.Pro307AlafsTer8
NM_001374820.1:c.918_919insG	NP_001361749.1:p.Pro307AlafsTer8
NM_001374828.1:c.918_919insG MANE Select	NP_001361757.1:p.Pro307AlafsTer8
NM_017519.3:c.918_919insG	NP_059989.3:p.Pro307AlafsTer8