Canonical Allele Identifier: CA366227579

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3428T>G	ENSP00000055163.8:p.Val1143Gly
ENST00000414678.8:c.3497T>G	ENSP00000412835.3:p.Val1166Gly
ENST00000637015.2:c.3716T>G	ENSP00000489729.2:p.Val1239Gly
ENST00000319584.11:c.1601T>G	ENSP00000313006.7:p.Val534Gly
ENST00000346085.10:c.3467T>G	ENSP00000344546.5:p.Val1156Gly
ENST00000350026.10:c.3179T>G	ENSP00000055163.7:p.Val1060Gly
ENST00000414678.7:c.1745T>G	ENSP00000412835.2:p.Val582Gly
ENST00000635849.1:c.908T>G	ENSP00000490948.1:p.Val303Gly
ENST00000635957.1:c.542T>G	ENSP00000490385.1:p.Val181Gly
ENST00000636930.2:c.3587T>G MANE Select	ENSP00000490491.2:p.Val1196Gly
ENST00000636940.1:n.1584T>G
ENST00000637015.1:c.955T>G
ENST00000637568.1:c.869T>G
ENST00000637741.1:n.253T>G
ENST00000637810.1:c.929T>G	ENSP00000489636.1:p.Val310Gly
ENST00000637904.1:c.1088T>G	ENSP00000490550.1:p.Val363Gly
ENST00000647938.1:c.3218T>G	ENSP00000498155.1:p.Val1073Gly
ENST00000319584.10:c.1604T>G	ENSP00000313006.6:p.Val535Gly
ENST00000346085.9:c.3218T>G	ENSP00000344546.4:p.Val1073Gly
ENST00000350026.9:c.3179T>G	ENSP00000055163.7:p.Val1060Gly
ENST00000400790.3:c.380T>G	ENSP00000383596.3:p.Val127Gly
ENST00000414678.6:c.1745T>G	ENSP00000412835.2:p.Val582Gly
ENST00000478761.3:c.789T>G
NM_017519.2:c.3179T>G	NP_059989.2:p.Val1060Gly
NM_020732.3:c.3218T>G	NP_065783.3:p.Val1073Gly
XM_005267069.3:c.3338T>G	XP_005267126.2:p.Val1113Gly
XM_011535984.1:c.2417T>G	XP_011534286.1:p.Val806Gly
XM_011535985.1:c.2237T>G	XP_011534287.1:p.Val746Gly
XM_011535986.1:c.1997T>G	XP_011534288.1:p.Val666Gly
XM_011535987.1:c.1616T>G	XP_011534289.1:p.Val539Gly
XM_011535988.1:c.479T>G	XP_011534290.1:p.Val160Gly
NM_001346813.1:c.3338T>G	NP_001333742.1:p.Val1113Gly
NM_001363725.1:c.1088T>G	NP_001350654.1:p.Val363Gly
XM_011535984.2:c.3548T>G	XP_011534286.2:p.Val1183Gly
XM_011535988.3:c.479T>G	XP_011534290.1:p.Val160Gly
XM_017011103.2:c.3449T>G	XP_016866592.1:p.Val1150Gly
XM_017011104.1:c.3419T>G	XP_016866593.1:p.Val1140Gly
XM_017011105.2:c.3389T>G	XP_016866594.1:p.Val1130Gly
XM_017011106.2:c.3260T>G	XP_016866595.1:p.Val1087Gly
XM_017011107.2:c.3239T>G	XP_016866596.1:p.Val1080Gly
XR_002956289.1:n.3631T>G
NM_001363725.2:c.1088T>G	NP_001350654.1:p.Val363Gly
NM_001371656.1:c.3467T>G	NP_001358585.1:p.Val1156Gly
NM_001374820.1:c.3467T>G	NP_001361749.1:p.Val1156Gly
NM_001374828.1:c.3587T>G MANE Select	NP_001361757.1:p.Val1196Gly
NM_017519.3:c.3428T>G	NP_059989.3:p.Val1143Gly