Canonical Allele Identifier: CA366240890

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521905A>G (hg19) ; chr6:g.157200771A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200771A>G , CM000668.2:g.157200771A>G	GRCh38
NC_000006.11:g.157521905A>G , CM000668.1:g.157521905A>G	GRCh37
NC_000006.10:g.157563597A>G	NCBI36
NG_032093.1:g.427842A>G
NG_032093.2:g.427842A>G
NG_066624.1:g.429746A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4387A>G	ENSP00000055163.8:p.Asn1463Asp
ENST00000414678.8:c.4456A>G	ENSP00000412835.3:p.Asn1486Asp
ENST00000637015.2:c.4675A>G	ENSP00000489729.2:p.Asn1559Asp
ENST00000346085.10:c.4426A>G	ENSP00000344546.5:p.Asn1476Asp
ENST00000350026.10:c.4138A>G	ENSP00000055163.7:p.Asn1380Asp
ENST00000414678.7:c.2704A>G	ENSP00000412835.2:p.Asn902Asp
ENST00000635849.1:c.1867A>G	ENSP00000490948.1:p.Asn623Asp
ENST00000635957.1:c.1498A>G	ENSP00000490385.1:p.Asn500Asp
ENST00000636227.1:n.3009A>G
ENST00000636254.1:n.466A>G
ENST00000636930.2:c.4546A>G MANE Select	ENSP00000490491.2:p.Asn1516Asp
ENST00000636940.1:n.2543A>G
ENST00000637015.1:c.1914A>G
ENST00000637568.1:c.1828A>G
ENST00000637741.1:n.1212A>G
ENST00000637810.1:c.1888A>G	ENSP00000489636.1:p.Asn630Asp
ENST00000637904.1:c.2047A>G	ENSP00000490550.1:p.Asn683Asp
ENST00000647938.1:c.4177A>G	ENSP00000498155.1:p.Asn1393Asp
ENST00000346085.9:c.4177A>G	ENSP00000344546.4:p.Asn1393Asp
ENST00000350026.9:c.4138A>G	ENSP00000055163.7:p.Asn1380Asp
ENST00000414678.6:c.2704A>G	ENSP00000412835.2:p.Asn902Asp
NM_017519.2:c.4138A>G	NP_059989.2:p.Asn1380Asp
NM_020732.3:c.4177A>G	NP_065783.3:p.Asn1393Asp
XM_005267069.3:c.4297A>G	XP_005267126.2:p.Asn1433Asp
XM_011535984.1:c.3376A>G	XP_011534286.1:p.Asn1126Asp
XM_011535985.1:c.3196A>G	XP_011534287.1:p.Asn1066Asp
XM_011535986.1:c.2956A>G	XP_011534288.1:p.Asn986Asp
XM_011535987.1:c.2575A>G	XP_011534289.1:p.Asn859Asp
XM_011535988.1:c.1438A>G	XP_011534290.1:p.Asn480Asp
NM_001346813.1:c.4297A>G	NP_001333742.1:p.Asn1433Asp
NM_001363725.1:c.2047A>G	NP_001350654.1:p.Asn683Asp
XM_011535984.2:c.4507A>G	XP_011534286.2:p.Asn1503Asp
XM_011535988.3:c.1438A>G	XP_011534290.1:p.Asn480Asp
XM_017011103.2:c.4408A>G	XP_016866592.1:p.Asn1470Asp
XM_017011104.1:c.4378A>G	XP_016866593.1:p.Asn1460Asp
XM_017011105.2:c.4348A>G	XP_016866594.1:p.Asn1450Asp
XM_017011106.2:c.4219A>G	XP_016866595.1:p.Asn1407Asp
XM_017011107.2:c.4198A>G	XP_016866596.1:p.Asn1400Asp
XR_002956289.1:n.4493A>G
NM_001363725.2:c.2047A>G	NP_001350654.1:p.Asn683Asp
NM_001371656.1:c.4426A>G	NP_001358585.1:p.Asn1476Asp
NM_001374820.1:c.4426A>G	NP_001361749.1:p.Asn1476Asp
NM_001374828.1:c.4546A>G MANE Select	NP_001361757.1:p.Asn1516Asp
NM_017519.3:c.4387A>G	NP_059989.3:p.Asn1463Asp