Canonical Allele Identifier: CA366235033

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190081-G-A
• MyVariant Identifiers: chr6:g.157511215G>A (hg19) ; chr6:g.157190081G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190081G>A , CM000668.2:g.157190081G>A	GRCh38
NC_000006.11:g.157511215G>A , CM000668.1:g.157511215G>A	GRCh37
NC_000006.10:g.157552907G>A	NCBI36
NG_032093.1:g.417152G>A
NG_032093.2:g.417152G>A
NG_066624.1:g.419056G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3943G>A	ENSP00000055163.8:p.Asp1315Asn
ENST00000414678.8:c.4012G>A	ENSP00000412835.3:p.Asp1338Asn
ENST00000637015.2:c.4231G>A	ENSP00000489729.2:p.Asp1411Asn
ENST00000346085.10:c.3982G>A	ENSP00000344546.5:p.Asp1328Asn
ENST00000350026.10:c.3694G>A	ENSP00000055163.7:p.Asp1232Asn
ENST00000414678.7:c.2260G>A	ENSP00000412835.2:p.Asp754Asn
ENST00000635849.1:c.1423G>A	ENSP00000490948.1:p.Asp475Asn
ENST00000635957.1:c.1054G>A	ENSP00000490385.1:p.Asp352Asn
ENST00000636930.2:c.4102G>A MANE Select	ENSP00000490491.2:p.Asp1368Asn
ENST00000636940.1:n.2099G>A
ENST00000637015.1:c.1470G>A
ENST00000637568.1:c.1384G>A
ENST00000637741.1:n.768G>A
ENST00000637810.1:c.1444G>A	ENSP00000489636.1:p.Asp482Asn
ENST00000637904.1:c.1603G>A	ENSP00000490550.1:p.Asp535Asn
ENST00000647938.1:c.3733G>A	ENSP00000498155.1:p.Asp1245Asn
ENST00000346085.9:c.3733G>A	ENSP00000344546.4:p.Asp1245Asn
ENST00000350026.9:c.3694G>A	ENSP00000055163.7:p.Asp1232Asn
ENST00000414678.6:c.2260G>A	ENSP00000412835.2:p.Asp754Asn
NM_017519.2:c.3694G>A	NP_059989.2:p.Asp1232Asn
NM_020732.3:c.3733G>A	NP_065783.3:p.Asp1245Asn
XM_005267069.3:c.3853G>A	XP_005267126.2:p.Asp1285Asn
XM_011535984.1:c.2932G>A	XP_011534286.1:p.Asp978Asn
XM_011535985.1:c.2752G>A	XP_011534287.1:p.Asp918Asn
XM_011535986.1:c.2512G>A	XP_011534288.1:p.Asp838Asn
XM_011535987.1:c.2131G>A	XP_011534289.1:p.Asp711Asn
XM_011535988.1:c.994G>A	XP_011534290.1:p.Asp332Asn
NM_001346813.1:c.3853G>A	NP_001333742.1:p.Asp1285Asn
NM_001363725.1:c.1603G>A	NP_001350654.1:p.Asp535Asn
XM_011535984.2:c.4063G>A	XP_011534286.2:p.Asp1355Asn
XM_011535988.3:c.994G>A	XP_011534290.1:p.Asp332Asn
XM_017011103.2:c.3964G>A	XP_016866592.1:p.Asp1322Asn
XM_017011104.1:c.3934G>A	XP_016866593.1:p.Asp1312Asn
XM_017011105.2:c.3904G>A	XP_016866594.1:p.Asp1302Asn
XM_017011106.2:c.3775G>A	XP_016866595.1:p.Asp1259Asn
XM_017011107.2:c.3754G>A	XP_016866596.1:p.Asp1252Asn
XR_002956289.1:n.4146G>A
NM_001363725.2:c.1603G>A	NP_001350654.1:p.Asp535Asn
NM_001371656.1:c.3982G>A	NP_001358585.1:p.Asp1328Asn
NM_001374820.1:c.3982G>A	NP_001361749.1:p.Asp1328Asn
NM_001374828.1:c.4102G>A MANE Select	NP_001361757.1:p.Asp1368Asn
NM_017519.3:c.3943G>A	NP_059989.3:p.Asp1315Asn