Canonical Allele Identifier: CA366227884

Gene: ARID1B

Linked Data

• dbSNP Id: rs753607488
• MyVariant Identifiers: chr6:g.157502215G>C (hg19) ; chr6:g.157181081G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181081G>C , CM000668.2:g.157181081G>C	GRCh38
NC_000006.11:g.157502215G>C , CM000668.1:g.157502215G>C	GRCh37
NC_000006.10:g.157543907G>C	NCBI36
NG_032093.1:g.408152G>C
NG_032093.2:g.408152G>C
NG_066624.1:g.410056G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3458G>C	ENSP00000055163.8:p.Arg1153Thr
ENST00000414678.8:c.3527G>C	ENSP00000412835.3:p.Arg1176Thr
ENST00000637015.2:c.3746G>C	ENSP00000489729.2:p.Arg1249Thr
ENST00000319584.11:c.1631G>C	ENSP00000313006.7:p.Arg544Thr
ENST00000346085.10:c.3497G>C	ENSP00000344546.5:p.Arg1166Thr
ENST00000350026.10:c.3209G>C	ENSP00000055163.7:p.Arg1070Thr
ENST00000414678.7:c.1775G>C	ENSP00000412835.2:p.Arg592Thr
ENST00000635849.1:c.938G>C	ENSP00000490948.1:p.Arg313Thr
ENST00000635957.1:c.572G>C	ENSP00000490385.1:p.Arg191Thr
ENST00000636930.2:c.3617G>C MANE Select	ENSP00000490491.2:p.Arg1206Thr
ENST00000636940.1:n.1614G>C
ENST00000637015.1:c.985G>C
ENST00000637568.1:c.899G>C
ENST00000637741.1:n.283G>C
ENST00000637810.1:c.959G>C	ENSP00000489636.1:p.Arg320Thr
ENST00000637904.1:c.1118G>C	ENSP00000490550.1:p.Arg373Thr
ENST00000647938.1:c.3248G>C	ENSP00000498155.1:p.Arg1083Thr
ENST00000319584.10:c.1634G>C	ENSP00000313006.6:p.Arg545Thr
ENST00000346085.9:c.3248G>C	ENSP00000344546.4:p.Arg1083Thr
ENST00000350026.9:c.3209G>C	ENSP00000055163.7:p.Arg1070Thr
ENST00000400790.3:c.410G>C	ENSP00000383596.3:p.Arg137Thr
ENST00000414678.6:c.1775G>C	ENSP00000412835.2:p.Arg592Thr
ENST00000478761.3:c.819G>C
NM_017519.2:c.3209G>C	NP_059989.2:p.Arg1070Thr
NM_020732.3:c.3248G>C	NP_065783.3:p.Arg1083Thr
XM_005267069.3:c.3368G>C	XP_005267126.2:p.Arg1123Thr
XM_011535984.1:c.2447G>C	XP_011534286.1:p.Arg816Thr
XM_011535985.1:c.2267G>C	XP_011534287.1:p.Arg756Thr
XM_011535986.1:c.2027G>C	XP_011534288.1:p.Arg676Thr
XM_011535987.1:c.1646G>C	XP_011534289.1:p.Arg549Thr
XM_011535988.1:c.509G>C	XP_011534290.1:p.Arg170Thr
NM_001346813.1:c.3368G>C	NP_001333742.1:p.Arg1123Thr
NM_001363725.1:c.1118G>C	NP_001350654.1:p.Arg373Thr
XM_011535984.2:c.3578G>C	XP_011534286.2:p.Arg1193Thr
XM_011535988.3:c.509G>C	XP_011534290.1:p.Arg170Thr
XM_017011103.2:c.3479G>C	XP_016866592.1:p.Arg1160Thr
XM_017011104.1:c.3449G>C	XP_016866593.1:p.Arg1150Thr
XM_017011105.2:c.3419G>C	XP_016866594.1:p.Arg1140Thr
XM_017011106.2:c.3290G>C	XP_016866595.1:p.Arg1097Thr
XM_017011107.2:c.3269G>C	XP_016866596.1:p.Arg1090Thr
XR_002956289.1:n.3661G>C
NM_001363725.2:c.1118G>C	NP_001350654.1:p.Arg373Thr
NM_001371656.1:c.3497G>C	NP_001358585.1:p.Arg1166Thr
NM_001374820.1:c.3497G>C	NP_001361749.1:p.Arg1166Thr
NM_001374828.1:c.3617G>C MANE Select	NP_001361757.1:p.Arg1206Thr
NM_017519.3:c.3458G>C	NP_059989.3:p.Arg1153Thr