Canonical Allele Identifier: CA366234742

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511188G>A (hg19) ; chr6:g.157190054G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190054G>A , CM000668.2:g.157190054G>A	GRCh38
NC_000006.11:g.157511188G>A , CM000668.1:g.157511188G>A	GRCh37
NC_000006.10:g.157552880G>A	NCBI36
NG_032093.1:g.417125G>A
NG_032093.2:g.417125G>A
NG_066624.1:g.419029G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3916G>A	ENSP00000055163.8:p.Val1306Met
ENST00000414678.8:c.3985G>A	ENSP00000412835.3:p.Val1329Met
ENST00000637015.2:c.4204G>A	ENSP00000489729.2:p.Val1402Met
ENST00000346085.10:c.3955G>A	ENSP00000344546.5:p.Val1319Met
ENST00000350026.10:c.3667G>A	ENSP00000055163.7:p.Val1223Met
ENST00000414678.7:c.2233G>A	ENSP00000412835.2:p.Val745Met
ENST00000635849.1:c.1396G>A	ENSP00000490948.1:p.Val466Met
ENST00000635957.1:c.1027G>A	ENSP00000490385.1:p.Val343Met
ENST00000636930.2:c.4075G>A MANE Select	ENSP00000490491.2:p.Val1359Met
ENST00000636940.1:n.2072G>A
ENST00000637015.1:c.1443G>A
ENST00000637568.1:c.1357G>A
ENST00000637741.1:n.741G>A
ENST00000637810.1:c.1417G>A	ENSP00000489636.1:p.Val473Met
ENST00000637904.1:c.1576G>A	ENSP00000490550.1:p.Val526Met
ENST00000647938.1:c.3706G>A	ENSP00000498155.1:p.Val1236Met
ENST00000346085.9:c.3706G>A	ENSP00000344546.4:p.Val1236Met
ENST00000350026.9:c.3667G>A	ENSP00000055163.7:p.Val1223Met
ENST00000414678.6:c.2233G>A	ENSP00000412835.2:p.Val745Met
NM_017519.2:c.3667G>A	NP_059989.2:p.Val1223Met
NM_020732.3:c.3706G>A	NP_065783.3:p.Val1236Met
XM_005267069.3:c.3826G>A	XP_005267126.2:p.Val1276Met
XM_011535984.1:c.2905G>A	XP_011534286.1:p.Val969Met
XM_011535985.1:c.2725G>A	XP_011534287.1:p.Val909Met
XM_011535986.1:c.2485G>A	XP_011534288.1:p.Val829Met
XM_011535987.1:c.2104G>A	XP_011534289.1:p.Val702Met
XM_011535988.1:c.967G>A	XP_011534290.1:p.Val323Met
NM_001346813.1:c.3826G>A	NP_001333742.1:p.Val1276Met
NM_001363725.1:c.1576G>A	NP_001350654.1:p.Val526Met
XM_011535984.2:c.4036G>A	XP_011534286.2:p.Val1346Met
XM_011535988.3:c.967G>A	XP_011534290.1:p.Val323Met
XM_017011103.2:c.3937G>A	XP_016866592.1:p.Val1313Met
XM_017011104.1:c.3907G>A	XP_016866593.1:p.Val1303Met
XM_017011105.2:c.3877G>A	XP_016866594.1:p.Val1293Met
XM_017011106.2:c.3748G>A	XP_016866595.1:p.Val1250Met
XM_017011107.2:c.3727G>A	XP_016866596.1:p.Val1243Met
XR_002956289.1:n.4119G>A
NM_001363725.2:c.1576G>A	NP_001350654.1:p.Val526Met
NM_001371656.1:c.3955G>A	NP_001358585.1:p.Val1319Met
NM_001374820.1:c.3955G>A	NP_001361749.1:p.Val1319Met
NM_001374828.1:c.4075G>A MANE Select	NP_001361757.1:p.Val1359Met
NM_017519.3:c.3916G>A	NP_059989.3:p.Val1306Met