Canonical Allele Identifier: CA366241423

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522135T>G (hg19) ; chr6:g.157201001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201001T>G , CM000668.2:g.157201001T>G	GRCh38
NC_000006.11:g.157522135T>G , CM000668.1:g.157522135T>G	GRCh37
NC_000006.10:g.157563827T>G	NCBI36
NG_032093.1:g.428072T>G
NG_032093.2:g.428072T>G
NG_066624.1:g.429976T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4617T>G	ENSP00000055163.8:p.Asn1539Lys
ENST00000414678.8:c.4686T>G	ENSP00000412835.3:p.Asn1562Lys
ENST00000637015.2:c.4905T>G	ENSP00000489729.2:p.Asn1635Lys
ENST00000346085.10:c.4656T>G	ENSP00000344546.5:p.Asn1552Lys
ENST00000350026.10:c.4368T>G	ENSP00000055163.7:p.Asn1456Lys
ENST00000414678.7:c.2934T>G	ENSP00000412835.2:p.Asn978Lys
ENST00000635849.1:c.2097T>G	ENSP00000490948.1:p.Asn699Lys
ENST00000635957.1:c.1728T>G	ENSP00000490385.1:p.Asn576Lys
ENST00000636227.1:n.3239T>G
ENST00000636254.1:n.696T>G
ENST00000636930.2:c.4776T>G MANE Select	ENSP00000490491.2:p.Asn1592Lys
ENST00000636940.1:n.2773T>G
ENST00000637015.1:c.2144T>G
ENST00000637568.1:c.2058T>G
ENST00000637741.1:n.1442T>G
ENST00000637810.1:c.2118T>G	ENSP00000489636.1:p.Asn706Lys
ENST00000637904.1:c.2277T>G	ENSP00000490550.1:p.Asn759Lys
ENST00000647938.1:c.4407T>G	ENSP00000498155.1:p.Asn1469Lys
ENST00000346085.9:c.4407T>G	ENSP00000344546.4:p.Asn1469Lys
ENST00000350026.9:c.4368T>G	ENSP00000055163.7:p.Asn1456Lys
ENST00000414678.6:c.2934T>G	ENSP00000412835.2:p.Asn978Lys
NM_017519.2:c.4368T>G	NP_059989.2:p.Asn1456Lys
NM_020732.3:c.4407T>G	NP_065783.3:p.Asn1469Lys
XM_005267069.3:c.4527T>G	XP_005267126.2:p.Asn1509Lys
XM_011535984.1:c.3606T>G	XP_011534286.1:p.Asn1202Lys
XM_011535985.1:c.3426T>G	XP_011534287.1:p.Asn1142Lys
XM_011535986.1:c.3186T>G	XP_011534288.1:p.Asn1062Lys
XM_011535987.1:c.2805T>G	XP_011534289.1:p.Asn935Lys
XM_011535988.1:c.1668T>G	XP_011534290.1:p.Asn556Lys
NM_001346813.1:c.4527T>G	NP_001333742.1:p.Asn1509Lys
NM_001363725.1:c.2277T>G	NP_001350654.1:p.Asn759Lys
XM_011535984.2:c.4737T>G	XP_011534286.2:p.Asn1579Lys
XM_011535988.3:c.1668T>G	XP_011534290.1:p.Asn556Lys
XM_017011103.2:c.4638T>G	XP_016866592.1:p.Asn1546Lys
XM_017011104.1:c.4608T>G	XP_016866593.1:p.Asn1536Lys
XM_017011105.2:c.4578T>G	XP_016866594.1:p.Asn1526Lys
XM_017011106.2:c.4449T>G	XP_016866595.1:p.Asn1483Lys
XM_017011107.2:c.4428T>G	XP_016866596.1:p.Asn1476Lys
XR_002956289.1:n.4723T>G
NM_001363725.2:c.2277T>G	NP_001350654.1:p.Asn759Lys
NM_001371656.1:c.4656T>G	NP_001358585.1:p.Asn1552Lys
NM_001374820.1:c.4656T>G	NP_001361749.1:p.Asn1552Lys
NM_001374828.1:c.4776T>G MANE Select	NP_001361757.1:p.Asn1592Lys
NM_017519.3:c.4617T>G	NP_059989.3:p.Asn1539Lys