Canonical Allele Identifier: CA366241564

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522158A>C (hg19) ; chr6:g.157201024A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201024A>C , CM000668.2:g.157201024A>C	GRCh38
NC_000006.11:g.157522158A>C , CM000668.1:g.157522158A>C	GRCh37
NC_000006.10:g.157563850A>C	NCBI36
NG_032093.1:g.428095A>C
NG_032093.2:g.428095A>C
NG_066624.1:g.429999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4640A>C	ENSP00000055163.8:p.Asn1547Thr
ENST00000414678.8:c.4709A>C	ENSP00000412835.3:p.Asn1570Thr
ENST00000637015.2:c.4928A>C	ENSP00000489729.2:p.Asn1643Thr
ENST00000346085.10:c.4679A>C	ENSP00000344546.5:p.Asn1560Thr
ENST00000350026.10:c.4391A>C	ENSP00000055163.7:p.Asn1464Thr
ENST00000414678.7:c.2957A>C	ENSP00000412835.2:p.Asn986Thr
ENST00000635849.1:c.2120A>C	ENSP00000490948.1:p.Asn707Thr
ENST00000635957.1:c.1751A>C	ENSP00000490385.1:p.Asn584Thr
ENST00000636227.1:n.3262A>C
ENST00000636254.1:n.719A>C
ENST00000636930.2:c.4799A>C MANE Select	ENSP00000490491.2:p.Asn1600Thr
ENST00000636940.1:n.2796A>C
ENST00000637015.1:c.2167A>C
ENST00000637568.1:c.2081A>C
ENST00000637741.1:n.1465A>C
ENST00000637810.1:c.2141A>C	ENSP00000489636.1:p.Asn714Thr
ENST00000637904.1:c.2300A>C	ENSP00000490550.1:p.Asn767Thr
ENST00000647938.1:c.4430A>C	ENSP00000498155.1:p.Asn1477Thr
ENST00000346085.9:c.4430A>C	ENSP00000344546.4:p.Asn1477Thr
ENST00000350026.9:c.4391A>C	ENSP00000055163.7:p.Asn1464Thr
ENST00000414678.6:c.2957A>C	ENSP00000412835.2:p.Asn986Thr
NM_017519.2:c.4391A>C	NP_059989.2:p.Asn1464Thr
NM_020732.3:c.4430A>C	NP_065783.3:p.Asn1477Thr
XM_005267069.3:c.4550A>C	XP_005267126.2:p.Asn1517Thr
XM_011535984.1:c.3629A>C	XP_011534286.1:p.Asn1210Thr
XM_011535985.1:c.3449A>C	XP_011534287.1:p.Asn1150Thr
XM_011535986.1:c.3209A>C	XP_011534288.1:p.Asn1070Thr
XM_011535987.1:c.2828A>C	XP_011534289.1:p.Asn943Thr
XM_011535988.1:c.1691A>C	XP_011534290.1:p.Asn564Thr
NM_001346813.1:c.4550A>C	NP_001333742.1:p.Asn1517Thr
NM_001363725.1:c.2300A>C	NP_001350654.1:p.Asn767Thr
XM_011535984.2:c.4760A>C	XP_011534286.2:p.Asn1587Thr
XM_011535988.3:c.1691A>C	XP_011534290.1:p.Asn564Thr
XM_017011103.2:c.4661A>C	XP_016866592.1:p.Asn1554Thr
XM_017011104.1:c.4631A>C	XP_016866593.1:p.Asn1544Thr
XM_017011105.2:c.4601A>C	XP_016866594.1:p.Asn1534Thr
XM_017011106.2:c.4472A>C	XP_016866595.1:p.Asn1491Thr
XM_017011107.2:c.4451A>C	XP_016866596.1:p.Asn1484Thr
XR_002956289.1:n.4746A>C
NM_001363725.2:c.2300A>C	NP_001350654.1:p.Asn767Thr
NM_001371656.1:c.4679A>C	NP_001358585.1:p.Asn1560Thr
NM_001374820.1:c.4679A>C	NP_001361749.1:p.Asn1560Thr
NM_001374828.1:c.4799A>C MANE Select	NP_001361757.1:p.Asn1600Thr
NM_017519.3:c.4640A>C	NP_059989.3:p.Asn1547Thr