Canonical Allele Identifier: CA366241338

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373721
• MyVariant Identifiers: chr6:g.157522104G>A (hg19) ; chr6:g.157200970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200970G>A , CM000668.2:g.157200970G>A	GRCh38
NC_000006.11:g.157522104G>A , CM000668.1:g.157522104G>A	GRCh37
NC_000006.10:g.157563796G>A	NCBI36
NG_032093.1:g.428041G>A
NG_032093.2:g.428041G>A
NG_066624.1:g.429945G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4586G>A	ENSP00000055163.8:p.Gly1529Glu
ENST00000414678.8:c.4655G>A	ENSP00000412835.3:p.Gly1552Glu
ENST00000637015.2:c.4874G>A	ENSP00000489729.2:p.Gly1625Glu
ENST00000346085.10:c.4625G>A	ENSP00000344546.5:p.Gly1542Glu
ENST00000350026.10:c.4337G>A	ENSP00000055163.7:p.Gly1446Glu
ENST00000414678.7:c.2903G>A	ENSP00000412835.2:p.Gly968Glu
ENST00000635849.1:c.2066G>A	ENSP00000490948.1:p.Gly689Glu
ENST00000635957.1:c.1697G>A	ENSP00000490385.1:p.Gly566Glu
ENST00000636227.1:n.3208G>A
ENST00000636254.1:n.665G>A
ENST00000636930.2:c.4745G>A MANE Select	ENSP00000490491.2:p.Gly1582Glu
ENST00000636940.1:n.2742G>A
ENST00000637015.1:c.2113G>A
ENST00000637568.1:c.2027G>A
ENST00000637741.1:n.1411G>A
ENST00000637810.1:c.2087G>A	ENSP00000489636.1:p.Gly696Glu
ENST00000637904.1:c.2246G>A	ENSP00000490550.1:p.Gly749Glu
ENST00000647938.1:c.4376G>A	ENSP00000498155.1:p.Gly1459Glu
ENST00000346085.9:c.4376G>A	ENSP00000344546.4:p.Gly1459Glu
ENST00000350026.9:c.4337G>A	ENSP00000055163.7:p.Gly1446Glu
ENST00000414678.6:c.2903G>A	ENSP00000412835.2:p.Gly968Glu
NM_017519.2:c.4337G>A	NP_059989.2:p.Gly1446Glu
NM_020732.3:c.4376G>A	NP_065783.3:p.Gly1459Glu
XM_005267069.3:c.4496G>A	XP_005267126.2:p.Gly1499Glu
XM_011535984.1:c.3575G>A	XP_011534286.1:p.Gly1192Glu
XM_011535985.1:c.3395G>A	XP_011534287.1:p.Gly1132Glu
XM_011535986.1:c.3155G>A	XP_011534288.1:p.Gly1052Glu
XM_011535987.1:c.2774G>A	XP_011534289.1:p.Gly925Glu
XM_011535988.1:c.1637G>A	XP_011534290.1:p.Gly546Glu
NM_001346813.1:c.4496G>A	NP_001333742.1:p.Gly1499Glu
NM_001363725.1:c.2246G>A	NP_001350654.1:p.Gly749Glu
XM_011535984.2:c.4706G>A	XP_011534286.2:p.Gly1569Glu
XM_011535988.3:c.1637G>A	XP_011534290.1:p.Gly546Glu
XM_017011103.2:c.4607G>A	XP_016866592.1:p.Gly1536Glu
XM_017011104.1:c.4577G>A	XP_016866593.1:p.Gly1526Glu
XM_017011105.2:c.4547G>A	XP_016866594.1:p.Gly1516Glu
XM_017011106.2:c.4418G>A	XP_016866595.1:p.Gly1473Glu
XM_017011107.2:c.4397G>A	XP_016866596.1:p.Gly1466Glu
XR_002956289.1:n.4692G>A
NM_001363725.2:c.2246G>A	NP_001350654.1:p.Gly749Glu
NM_001371656.1:c.4625G>A	NP_001358585.1:p.Gly1542Glu
NM_001374820.1:c.4625G>A	NP_001361749.1:p.Gly1542Glu
NM_001374828.1:c.4745G>A MANE Select	NP_001361757.1:p.Gly1582Glu
NM_017519.3:c.4586G>A	NP_059989.3:p.Gly1529Glu