Canonical Allele Identifier: CA452935971

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128211084
• MyVariant Identifiers: chr6:g.157222650G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901516G>A , CM000668.2:g.156901516G>A	GRCh38
NC_000006.11:g.157222650G>A , CM000668.1:g.157222650G>A	GRCh37
NC_000006.10:g.157264342G>A	NCBI36
NG_032093.1:g.128587G>A
NG_032093.2:g.128587G>A
NG_066624.1:g.130491G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2127G>A	ENSP00000055163.8:p.Gln709=
ENST00000414678.8:c.2127G>A	ENSP00000412835.3:p.Gln709=
ENST00000637015.2:c.2127G>A	ENSP00000489729.2:p.Gln709=
ENST00000319584.11:c.141G>A	ENSP00000313006.7:p.Gln47=
ENST00000346085.10:c.2166G>A	ENSP00000344546.5:p.Gln722=
ENST00000350026.10:c.1878G>A	ENSP00000055163.7:p.Gln626=
ENST00000414678.7:c.375G>A	ENSP00000412835.2:p.Gln125=
ENST00000636205.1:n.190G>A
ENST00000636748.1:c.408G>A	ENSP00000489917.1:p.Gln136=
ENST00000636930.2:c.2127G>A MANE Select	ENSP00000490491.2:p.Gln709=
ENST00000637532.1:c.153G>A	ENSP00000490420.1:p.Gln51=
ENST00000638000.1:c.344G>A
ENST00000647938.1:c.1917G>A	ENSP00000498155.1:p.Gln639=
ENST00000674190.1:n.834G>A
ENST00000674298.1:c.1867G>A
ENST00000319584.10:c.144G>A	ENSP00000313006.6:p.Gln48=
ENST00000346085.9:c.1917G>A	ENSP00000344546.4:p.Gln639=
ENST00000350026.9:c.1878G>A	ENSP00000055163.7:p.Gln626=
ENST00000414678.6:c.375G>A	ENSP00000412835.2:p.Gln125=
NM_017519.2:c.1878G>A	NP_059989.2:p.Gln626=
NM_020732.3:c.1917G>A	NP_065783.3:p.Gln639=
XM_005267069.3:c.1878G>A	XP_005267126.2:p.Gln626=
XM_011535984.1:c.786G>A	XP_011534286.1:p.Gln262=
XM_011535985.1:c.786G>A	XP_011534287.1:p.Gln262=
XM_011535986.1:c.366G>A	XP_011534288.1:p.Gln122=
NM_001346813.1:c.1878G>A	NP_001333742.1:p.Gln626=
XM_011535984.2:c.1917G>A	XP_011534286.2:p.Gln639=
XM_017011103.2:c.1917G>A	XP_016866592.1:p.Gln639=
XM_017011104.1:c.1917G>A	XP_016866593.1:p.Gln639=
XM_017011105.2:c.1917G>A	XP_016866594.1:p.Gln639=
XM_017011106.2:c.1917G>A	XP_016866595.1:p.Gln639=
XM_017011107.2:c.1917G>A	XP_016866596.1:p.Gln639=
XR_002956289.1:n.2000G>A
NM_001371656.1:c.2166G>A	NP_001358585.1:p.Gln722=
NM_001374820.1:c.2166G>A	NP_001361749.1:p.Gln722=
NM_001374828.1:c.2127G>A MANE Select	NP_001361757.1:p.Gln709=
NM_017519.3:c.2127G>A	NP_059989.3:p.Gln709=