Canonical Allele Identifier: CA366241412

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522134A>C (hg19) ; chr6:g.157201000A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201000A>C , CM000668.2:g.157201000A>C	GRCh38
NC_000006.11:g.157522134A>C , CM000668.1:g.157522134A>C	GRCh37
NC_000006.10:g.157563826A>C	NCBI36
NG_032093.1:g.428071A>C
NG_032093.2:g.428071A>C
NG_066624.1:g.429975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4616A>C	ENSP00000055163.8:p.Asn1539Thr
ENST00000414678.8:c.4685A>C	ENSP00000412835.3:p.Asn1562Thr
ENST00000637015.2:c.4904A>C	ENSP00000489729.2:p.Asn1635Thr
ENST00000346085.10:c.4655A>C	ENSP00000344546.5:p.Asn1552Thr
ENST00000350026.10:c.4367A>C	ENSP00000055163.7:p.Asn1456Thr
ENST00000414678.7:c.2933A>C	ENSP00000412835.2:p.Asn978Thr
ENST00000635849.1:c.2096A>C	ENSP00000490948.1:p.Asn699Thr
ENST00000635957.1:c.1727A>C	ENSP00000490385.1:p.Asn576Thr
ENST00000636227.1:n.3238A>C
ENST00000636254.1:n.695A>C
ENST00000636930.2:c.4775A>C MANE Select	ENSP00000490491.2:p.Asn1592Thr
ENST00000636940.1:n.2772A>C
ENST00000637015.1:c.2143A>C
ENST00000637568.1:c.2057A>C
ENST00000637741.1:n.1441A>C
ENST00000637810.1:c.2117A>C	ENSP00000489636.1:p.Asn706Thr
ENST00000637904.1:c.2276A>C	ENSP00000490550.1:p.Asn759Thr
ENST00000647938.1:c.4406A>C	ENSP00000498155.1:p.Asn1469Thr
ENST00000346085.9:c.4406A>C	ENSP00000344546.4:p.Asn1469Thr
ENST00000350026.9:c.4367A>C	ENSP00000055163.7:p.Asn1456Thr
ENST00000414678.6:c.2933A>C	ENSP00000412835.2:p.Asn978Thr
NM_017519.2:c.4367A>C	NP_059989.2:p.Asn1456Thr
NM_020732.3:c.4406A>C	NP_065783.3:p.Asn1469Thr
XM_005267069.3:c.4526A>C	XP_005267126.2:p.Asn1509Thr
XM_011535984.1:c.3605A>C	XP_011534286.1:p.Asn1202Thr
XM_011535985.1:c.3425A>C	XP_011534287.1:p.Asn1142Thr
XM_011535986.1:c.3185A>C	XP_011534288.1:p.Asn1062Thr
XM_011535987.1:c.2804A>C	XP_011534289.1:p.Asn935Thr
XM_011535988.1:c.1667A>C	XP_011534290.1:p.Asn556Thr
NM_001346813.1:c.4526A>C	NP_001333742.1:p.Asn1509Thr
NM_001363725.1:c.2276A>C	NP_001350654.1:p.Asn759Thr
XM_011535984.2:c.4736A>C	XP_011534286.2:p.Asn1579Thr
XM_011535988.3:c.1667A>C	XP_011534290.1:p.Asn556Thr
XM_017011103.2:c.4637A>C	XP_016866592.1:p.Asn1546Thr
XM_017011104.1:c.4607A>C	XP_016866593.1:p.Asn1536Thr
XM_017011105.2:c.4577A>C	XP_016866594.1:p.Asn1526Thr
XM_017011106.2:c.4448A>C	XP_016866595.1:p.Asn1483Thr
XM_017011107.2:c.4427A>C	XP_016866596.1:p.Asn1476Thr
XR_002956289.1:n.4722A>C
NM_001363725.2:c.2276A>C	NP_001350654.1:p.Asn759Thr
NM_001371656.1:c.4655A>C	NP_001358585.1:p.Asn1552Thr
NM_001374820.1:c.4655A>C	NP_001361749.1:p.Asn1552Thr
NM_001374828.1:c.4775A>C MANE Select	NP_001361757.1:p.Asn1592Thr
NM_017519.3:c.4616A>C	NP_059989.3:p.Asn1539Thr