Canonical Allele Identifier: CA366234951

Gene: ARID1B

Linked Data

• COSMIC: COSM450797 ; COSM1487407
• MyVariant Identifiers: chr6:g.157511206G>C (hg19) ; chr6:g.157190072G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190072G>C , CM000668.2:g.157190072G>C	GRCh38
NC_000006.11:g.157511206G>C , CM000668.1:g.157511206G>C	GRCh37
NC_000006.10:g.157552898G>C	NCBI36
NG_032093.1:g.417143G>C
NG_032093.2:g.417143G>C
NG_066624.1:g.419047G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3934G>C	ENSP00000055163.8:p.Asp1312His
ENST00000414678.8:c.4003G>C	ENSP00000412835.3:p.Asp1335His
ENST00000637015.2:c.4222G>C	ENSP00000489729.2:p.Asp1408His
ENST00000346085.10:c.3973G>C	ENSP00000344546.5:p.Asp1325His
ENST00000350026.10:c.3685G>C	ENSP00000055163.7:p.Asp1229His
ENST00000414678.7:c.2251G>C	ENSP00000412835.2:p.Asp751His
ENST00000635849.1:c.1414G>C	ENSP00000490948.1:p.Asp472His
ENST00000635957.1:c.1045G>C	ENSP00000490385.1:p.Asp349His
ENST00000636930.2:c.4093G>C MANE Select	ENSP00000490491.2:p.Asp1365His
ENST00000636940.1:n.2090G>C
ENST00000637015.1:c.1461G>C
ENST00000637568.1:c.1375G>C
ENST00000637741.1:n.759G>C
ENST00000637810.1:c.1435G>C	ENSP00000489636.1:p.Asp479His
ENST00000637904.1:c.1594G>C	ENSP00000490550.1:p.Asp532His
ENST00000647938.1:c.3724G>C	ENSP00000498155.1:p.Asp1242His
ENST00000346085.9:c.3724G>C	ENSP00000344546.4:p.Asp1242His
ENST00000350026.9:c.3685G>C	ENSP00000055163.7:p.Asp1229His
ENST00000414678.6:c.2251G>C	ENSP00000412835.2:p.Asp751His
NM_017519.2:c.3685G>C	NP_059989.2:p.Asp1229His
NM_020732.3:c.3724G>C	NP_065783.3:p.Asp1242His
XM_005267069.3:c.3844G>C	XP_005267126.2:p.Asp1282His
XM_011535984.1:c.2923G>C	XP_011534286.1:p.Asp975His
XM_011535985.1:c.2743G>C	XP_011534287.1:p.Asp915His
XM_011535986.1:c.2503G>C	XP_011534288.1:p.Asp835His
XM_011535987.1:c.2122G>C	XP_011534289.1:p.Asp708His
XM_011535988.1:c.985G>C	XP_011534290.1:p.Asp329His
NM_001346813.1:c.3844G>C	NP_001333742.1:p.Asp1282His
NM_001363725.1:c.1594G>C	NP_001350654.1:p.Asp532His
XM_011535984.2:c.4054G>C	XP_011534286.2:p.Asp1352His
XM_011535988.3:c.985G>C	XP_011534290.1:p.Asp329His
XM_017011103.2:c.3955G>C	XP_016866592.1:p.Asp1319His
XM_017011104.1:c.3925G>C	XP_016866593.1:p.Asp1309His
XM_017011105.2:c.3895G>C	XP_016866594.1:p.Asp1299His
XM_017011106.2:c.3766G>C	XP_016866595.1:p.Asp1256His
XM_017011107.2:c.3745G>C	XP_016866596.1:p.Asp1249His
XR_002956289.1:n.4137G>C
NM_001363725.2:c.1594G>C	NP_001350654.1:p.Asp532His
NM_001371656.1:c.3973G>C	NP_001358585.1:p.Asp1325His
NM_001374820.1:c.3973G>C	NP_001361749.1:p.Asp1325His
NM_001374828.1:c.4093G>C MANE Select	NP_001361757.1:p.Asp1365His
NM_017519.3:c.3934G>C	NP_059989.3:p.Asp1312His