Canonical Allele Identifier: CA366234784

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511191C>A (hg19) ; chr6:g.157190057C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190057C>A , CM000668.2:g.157190057C>A	GRCh38
NC_000006.11:g.157511191C>A , CM000668.1:g.157511191C>A	GRCh37
NC_000006.10:g.157552883C>A	NCBI36
NG_032093.1:g.417128C>A
NG_032093.2:g.417128C>A
NG_066624.1:g.419032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3919C>A	ENSP00000055163.8:p.His1307Asn
ENST00000414678.8:c.3988C>A	ENSP00000412835.3:p.His1330Asn
ENST00000637015.2:c.4207C>A	ENSP00000489729.2:p.His1403Asn
ENST00000346085.10:c.3958C>A	ENSP00000344546.5:p.His1320Asn
ENST00000350026.10:c.3670C>A	ENSP00000055163.7:p.His1224Asn
ENST00000414678.7:c.2236C>A	ENSP00000412835.2:p.His746Asn
ENST00000635849.1:c.1399C>A	ENSP00000490948.1:p.His467Asn
ENST00000635957.1:c.1030C>A	ENSP00000490385.1:p.His344Asn
ENST00000636930.2:c.4078C>A MANE Select	ENSP00000490491.2:p.His1360Asn
ENST00000636940.1:n.2075C>A
ENST00000637015.1:c.1446C>A
ENST00000637568.1:c.1360C>A
ENST00000637741.1:n.744C>A
ENST00000637810.1:c.1420C>A	ENSP00000489636.1:p.His474Asn
ENST00000637904.1:c.1579C>A	ENSP00000490550.1:p.His527Asn
ENST00000647938.1:c.3709C>A	ENSP00000498155.1:p.His1237Asn
ENST00000346085.9:c.3709C>A	ENSP00000344546.4:p.His1237Asn
ENST00000350026.9:c.3670C>A	ENSP00000055163.7:p.His1224Asn
ENST00000414678.6:c.2236C>A	ENSP00000412835.2:p.His746Asn
NM_017519.2:c.3670C>A	NP_059989.2:p.His1224Asn
NM_020732.3:c.3709C>A	NP_065783.3:p.His1237Asn
XM_005267069.3:c.3829C>A	XP_005267126.2:p.His1277Asn
XM_011535984.1:c.2908C>A	XP_011534286.1:p.His970Asn
XM_011535985.1:c.2728C>A	XP_011534287.1:p.His910Asn
XM_011535986.1:c.2488C>A	XP_011534288.1:p.His830Asn
XM_011535987.1:c.2107C>A	XP_011534289.1:p.His703Asn
XM_011535988.1:c.970C>A	XP_011534290.1:p.His324Asn
NM_001346813.1:c.3829C>A	NP_001333742.1:p.His1277Asn
NM_001363725.1:c.1579C>A	NP_001350654.1:p.His527Asn
XM_011535984.2:c.4039C>A	XP_011534286.2:p.His1347Asn
XM_011535988.3:c.970C>A	XP_011534290.1:p.His324Asn
XM_017011103.2:c.3940C>A	XP_016866592.1:p.His1314Asn
XM_017011104.1:c.3910C>A	XP_016866593.1:p.His1304Asn
XM_017011105.2:c.3880C>A	XP_016866594.1:p.His1294Asn
XM_017011106.2:c.3751C>A	XP_016866595.1:p.His1251Asn
XM_017011107.2:c.3730C>A	XP_016866596.1:p.His1244Asn
XR_002956289.1:n.4122C>A
NM_001363725.2:c.1579C>A	NP_001350654.1:p.His527Asn
NM_001371656.1:c.3958C>A	NP_001358585.1:p.His1320Asn
NM_001374820.1:c.3958C>A	NP_001361749.1:p.His1320Asn
NM_001374828.1:c.4078C>A MANE Select	NP_001361757.1:p.His1360Asn
NM_017519.3:c.3919C>A	NP_059989.3:p.His1307Asn