Canonical Allele Identifier: CA366234787

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3919C>G	ENSP00000055163.8:p.His1307Asp
ENST00000414678.8:c.3988C>G	ENSP00000412835.3:p.His1330Asp
ENST00000637015.2:c.4207C>G	ENSP00000489729.2:p.His1403Asp
ENST00000346085.10:c.3958C>G	ENSP00000344546.5:p.His1320Asp
ENST00000350026.10:c.3670C>G	ENSP00000055163.7:p.His1224Asp
ENST00000414678.7:c.2236C>G	ENSP00000412835.2:p.His746Asp
ENST00000635849.1:c.1399C>G	ENSP00000490948.1:p.His467Asp
ENST00000635957.1:c.1030C>G	ENSP00000490385.1:p.His344Asp
ENST00000636930.2:c.4078C>G MANE Select	ENSP00000490491.2:p.His1360Asp
ENST00000636940.1:n.2075C>G
ENST00000637015.1:c.1446C>G
ENST00000637568.1:c.1360C>G
ENST00000637741.1:n.744C>G
ENST00000637810.1:c.1420C>G	ENSP00000489636.1:p.His474Asp
ENST00000637904.1:c.1579C>G	ENSP00000490550.1:p.His527Asp
ENST00000647938.1:c.3709C>G	ENSP00000498155.1:p.His1237Asp
ENST00000346085.9:c.3709C>G	ENSP00000344546.4:p.His1237Asp
ENST00000350026.9:c.3670C>G	ENSP00000055163.7:p.His1224Asp
ENST00000414678.6:c.2236C>G	ENSP00000412835.2:p.His746Asp
NM_017519.2:c.3670C>G	NP_059989.2:p.His1224Asp
NM_020732.3:c.3709C>G	NP_065783.3:p.His1237Asp
XM_005267069.3:c.3829C>G	XP_005267126.2:p.His1277Asp
XM_011535984.1:c.2908C>G	XP_011534286.1:p.His970Asp
XM_011535985.1:c.2728C>G	XP_011534287.1:p.His910Asp
XM_011535986.1:c.2488C>G	XP_011534288.1:p.His830Asp
XM_011535987.1:c.2107C>G	XP_011534289.1:p.His703Asp
XM_011535988.1:c.970C>G	XP_011534290.1:p.His324Asp
NM_001346813.1:c.3829C>G	NP_001333742.1:p.His1277Asp
NM_001363725.1:c.1579C>G	NP_001350654.1:p.His527Asp
XM_011535984.2:c.4039C>G	XP_011534286.2:p.His1347Asp
XM_011535988.3:c.970C>G	XP_011534290.1:p.His324Asp
XM_017011103.2:c.3940C>G	XP_016866592.1:p.His1314Asp
XM_017011104.1:c.3910C>G	XP_016866593.1:p.His1304Asp
XM_017011105.2:c.3880C>G	XP_016866594.1:p.His1294Asp
XM_017011106.2:c.3751C>G	XP_016866595.1:p.His1251Asp
XM_017011107.2:c.3730C>G	XP_016866596.1:p.His1244Asp
XR_002956289.1:n.4122C>G
NM_001363725.2:c.1579C>G	NP_001350654.1:p.His527Asp
NM_001371656.1:c.3958C>G	NP_001358585.1:p.His1320Asp
NM_001374820.1:c.3958C>G	NP_001361749.1:p.His1320Asp
NM_001374828.1:c.4078C>G MANE Select	NP_001361757.1:p.His1360Asp
NM_017519.3:c.3919C>G	NP_059989.3:p.His1307Asp