Canonical Allele Identifier: CA366227571

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317076
• MyVariant Identifiers: chr6:g.157502185T>A (hg19) ; chr6:g.157181051T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181051T>A , CM000668.2:g.157181051T>A	GRCh38
NC_000006.11:g.157502185T>A , CM000668.1:g.157502185T>A	GRCh37
NC_000006.10:g.157543877T>A	NCBI36
NG_032093.1:g.408122T>A
NG_032093.2:g.408122T>A
NG_066624.1:g.410026T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3428T>A	ENSP00000055163.8:p.Val1143Asp
ENST00000414678.8:c.3497T>A	ENSP00000412835.3:p.Val1166Asp
ENST00000637015.2:c.3716T>A	ENSP00000489729.2:p.Val1239Asp
ENST00000319584.11:c.1601T>A	ENSP00000313006.7:p.Val534Asp
ENST00000346085.10:c.3467T>A	ENSP00000344546.5:p.Val1156Asp
ENST00000350026.10:c.3179T>A	ENSP00000055163.7:p.Val1060Asp
ENST00000414678.7:c.1745T>A	ENSP00000412835.2:p.Val582Asp
ENST00000635849.1:c.908T>A	ENSP00000490948.1:p.Val303Asp
ENST00000635957.1:c.542T>A	ENSP00000490385.1:p.Val181Asp
ENST00000636930.2:c.3587T>A MANE Select	ENSP00000490491.2:p.Val1196Asp
ENST00000636940.1:n.1584T>A
ENST00000637015.1:c.955T>A
ENST00000637568.1:c.869T>A
ENST00000637741.1:n.253T>A
ENST00000637810.1:c.929T>A	ENSP00000489636.1:p.Val310Asp
ENST00000637904.1:c.1088T>A	ENSP00000490550.1:p.Val363Asp
ENST00000647938.1:c.3218T>A	ENSP00000498155.1:p.Val1073Asp
ENST00000319584.10:c.1604T>A	ENSP00000313006.6:p.Val535Asp
ENST00000346085.9:c.3218T>A	ENSP00000344546.4:p.Val1073Asp
ENST00000350026.9:c.3179T>A	ENSP00000055163.7:p.Val1060Asp
ENST00000400790.3:c.380T>A	ENSP00000383596.3:p.Val127Asp
ENST00000414678.6:c.1745T>A	ENSP00000412835.2:p.Val582Asp
ENST00000478761.3:c.789T>A
NM_017519.2:c.3179T>A	NP_059989.2:p.Val1060Asp
NM_020732.3:c.3218T>A	NP_065783.3:p.Val1073Asp
XM_005267069.3:c.3338T>A	XP_005267126.2:p.Val1113Asp
XM_011535984.1:c.2417T>A	XP_011534286.1:p.Val806Asp
XM_011535985.1:c.2237T>A	XP_011534287.1:p.Val746Asp
XM_011535986.1:c.1997T>A	XP_011534288.1:p.Val666Asp
XM_011535987.1:c.1616T>A	XP_011534289.1:p.Val539Asp
XM_011535988.1:c.479T>A	XP_011534290.1:p.Val160Asp
NM_001346813.1:c.3338T>A	NP_001333742.1:p.Val1113Asp
NM_001363725.1:c.1088T>A	NP_001350654.1:p.Val363Asp
XM_011535984.2:c.3548T>A	XP_011534286.2:p.Val1183Asp
XM_011535988.3:c.479T>A	XP_011534290.1:p.Val160Asp
XM_017011103.2:c.3449T>A	XP_016866592.1:p.Val1150Asp
XM_017011104.1:c.3419T>A	XP_016866593.1:p.Val1140Asp
XM_017011105.2:c.3389T>A	XP_016866594.1:p.Val1130Asp
XM_017011106.2:c.3260T>A	XP_016866595.1:p.Val1087Asp
XM_017011107.2:c.3239T>A	XP_016866596.1:p.Val1080Asp
XR_002956289.1:n.3631T>A
NM_001363725.2:c.1088T>A	NP_001350654.1:p.Val363Asp
NM_001371656.1:c.3467T>A	NP_001358585.1:p.Val1156Asp
NM_001374820.1:c.3467T>A	NP_001361749.1:p.Val1156Asp
NM_001374828.1:c.3587T>A MANE Select	NP_001361757.1:p.Val1196Asp
NM_017519.3:c.3428T>A	NP_059989.3:p.Val1143Asp