Canonical Allele Identifier: CA366227642

Gene: ARID1B

Linked Data

• dbSNP Id: rs1583463667
• MyVariant Identifiers: chr6:g.157502194A>C (hg19) ; chr6:g.157181060A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181060A>C , CM000668.2:g.157181060A>C	GRCh38
NC_000006.11:g.157502194A>C , CM000668.1:g.157502194A>C	GRCh37
NC_000006.10:g.157543886A>C	NCBI36
NG_032093.1:g.408131A>C
NG_032093.2:g.408131A>C
NG_066624.1:g.410035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3437A>C	ENSP00000055163.8:p.Tyr1146Ser
ENST00000414678.8:c.3506A>C	ENSP00000412835.3:p.Tyr1169Ser
ENST00000637015.2:c.3725A>C	ENSP00000489729.2:p.Tyr1242Ser
ENST00000319584.11:c.1610A>C	ENSP00000313006.7:p.Tyr537Ser
ENST00000346085.10:c.3476A>C	ENSP00000344546.5:p.Tyr1159Ser
ENST00000350026.10:c.3188A>C	ENSP00000055163.7:p.Tyr1063Ser
ENST00000414678.7:c.1754A>C	ENSP00000412835.2:p.Tyr585Ser
ENST00000635849.1:c.917A>C	ENSP00000490948.1:p.Tyr306Ser
ENST00000635957.1:c.551A>C	ENSP00000490385.1:p.Tyr184Ser
ENST00000636930.2:c.3596A>C MANE Select	ENSP00000490491.2:p.Tyr1199Ser
ENST00000636940.1:n.1593A>C
ENST00000637015.1:c.964A>C
ENST00000637568.1:c.878A>C
ENST00000637741.1:n.262A>C
ENST00000637810.1:c.938A>C	ENSP00000489636.1:p.Tyr313Ser
ENST00000637904.1:c.1097A>C	ENSP00000490550.1:p.Tyr366Ser
ENST00000647938.1:c.3227A>C	ENSP00000498155.1:p.Tyr1076Ser
ENST00000319584.10:c.1613A>C	ENSP00000313006.6:p.Tyr538Ser
ENST00000346085.9:c.3227A>C	ENSP00000344546.4:p.Tyr1076Ser
ENST00000350026.9:c.3188A>C	ENSP00000055163.7:p.Tyr1063Ser
ENST00000400790.3:c.389A>C	ENSP00000383596.3:p.Tyr130Ser
ENST00000414678.6:c.1754A>C	ENSP00000412835.2:p.Tyr585Ser
ENST00000478761.3:c.798A>C
NM_017519.2:c.3188A>C	NP_059989.2:p.Tyr1063Ser
NM_020732.3:c.3227A>C	NP_065783.3:p.Tyr1076Ser
XM_005267069.3:c.3347A>C	XP_005267126.2:p.Tyr1116Ser
XM_011535984.1:c.2426A>C	XP_011534286.1:p.Tyr809Ser
XM_011535985.1:c.2246A>C	XP_011534287.1:p.Tyr749Ser
XM_011535986.1:c.2006A>C	XP_011534288.1:p.Tyr669Ser
XM_011535987.1:c.1625A>C	XP_011534289.1:p.Tyr542Ser
XM_011535988.1:c.488A>C	XP_011534290.1:p.Tyr163Ser
NM_001346813.1:c.3347A>C	NP_001333742.1:p.Tyr1116Ser
NM_001363725.1:c.1097A>C	NP_001350654.1:p.Tyr366Ser
XM_011535984.2:c.3557A>C	XP_011534286.2:p.Tyr1186Ser
XM_011535988.3:c.488A>C	XP_011534290.1:p.Tyr163Ser
XM_017011103.2:c.3458A>C	XP_016866592.1:p.Tyr1153Ser
XM_017011104.1:c.3428A>C	XP_016866593.1:p.Tyr1143Ser
XM_017011105.2:c.3398A>C	XP_016866594.1:p.Tyr1133Ser
XM_017011106.2:c.3269A>C	XP_016866595.1:p.Tyr1090Ser
XM_017011107.2:c.3248A>C	XP_016866596.1:p.Tyr1083Ser
XR_002956289.1:n.3640A>C
NM_001363725.2:c.1097A>C	NP_001350654.1:p.Tyr366Ser
NM_001371656.1:c.3476A>C	NP_001358585.1:p.Tyr1159Ser
NM_001374820.1:c.3476A>C	NP_001361749.1:p.Tyr1159Ser
NM_001374828.1:c.3596A>C MANE Select	NP_001361757.1:p.Tyr1199Ser
NM_017519.3:c.3437A>C	NP_059989.3:p.Tyr1146Ser