Canonical Allele Identifier: CA366227455

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2309270
• ClinVar RCV Id: RCV002887057
• dbSNP Id: rs2128316990
• MyVariant Identifiers: chr6:g.157502173G>A (hg19) ; chr6:g.157181039G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181039G>A , CM000668.2:g.157181039G>A	GRCh38
NC_000006.11:g.157502173G>A , CM000668.1:g.157502173G>A	GRCh37
NC_000006.10:g.157543865G>A	NCBI36
NG_032093.1:g.408110G>A
NG_032093.2:g.408110G>A
NG_066624.1:g.410014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3416G>A	ENSP00000055163.8:p.Arg1139Lys
ENST00000414678.8:c.3485G>A	ENSP00000412835.3:p.Arg1162Lys
ENST00000637015.2:c.3704G>A	ENSP00000489729.2:p.Arg1235Lys
ENST00000319584.11:c.1589G>A	ENSP00000313006.7:p.Arg530Lys
ENST00000346085.10:c.3455G>A	ENSP00000344546.5:p.Arg1152Lys
ENST00000350026.10:c.3167G>A	ENSP00000055163.7:p.Arg1056Lys
ENST00000414678.7:c.1733G>A	ENSP00000412835.2:p.Arg578Lys
ENST00000635849.1:c.896G>A	ENSP00000490948.1:p.Arg299Lys
ENST00000635957.1:c.530G>A	ENSP00000490385.1:p.Arg177Lys
ENST00000636930.2:c.3575G>A MANE Select	ENSP00000490491.2:p.Arg1192Lys
ENST00000636940.1:n.1572G>A
ENST00000637015.1:c.943G>A
ENST00000637568.1:c.857G>A
ENST00000637741.1:n.241G>A
ENST00000637810.1:c.917G>A	ENSP00000489636.1:p.Arg306Lys
ENST00000637904.1:c.1076G>A	ENSP00000490550.1:p.Arg359Lys
ENST00000647938.1:c.3206G>A	ENSP00000498155.1:p.Arg1069Lys
ENST00000319584.10:c.1592G>A	ENSP00000313006.6:p.Arg531Lys
ENST00000346085.9:c.3206G>A	ENSP00000344546.4:p.Arg1069Lys
ENST00000350026.9:c.3167G>A	ENSP00000055163.7:p.Arg1056Lys
ENST00000400790.3:c.368G>A	ENSP00000383596.3:p.Arg123Lys
ENST00000414678.6:c.1733G>A	ENSP00000412835.2:p.Arg578Lys
ENST00000478761.3:c.777G>A
NM_017519.2:c.3167G>A	NP_059989.2:p.Arg1056Lys
NM_020732.3:c.3206G>A	NP_065783.3:p.Arg1069Lys
XM_005267069.3:c.3326G>A	XP_005267126.2:p.Arg1109Lys
XM_011535984.1:c.2405G>A	XP_011534286.1:p.Arg802Lys
XM_011535985.1:c.2225G>A	XP_011534287.1:p.Arg742Lys
XM_011535986.1:c.1985G>A	XP_011534288.1:p.Arg662Lys
XM_011535987.1:c.1604G>A	XP_011534289.1:p.Arg535Lys
XM_011535988.1:c.467G>A	XP_011534290.1:p.Arg156Lys
NM_001346813.1:c.3326G>A	NP_001333742.1:p.Arg1109Lys
NM_001363725.1:c.1076G>A	NP_001350654.1:p.Arg359Lys
XM_011535984.2:c.3536G>A	XP_011534286.2:p.Arg1179Lys
XM_011535988.3:c.467G>A	XP_011534290.1:p.Arg156Lys
XM_017011103.2:c.3437G>A	XP_016866592.1:p.Arg1146Lys
XM_017011104.1:c.3407G>A	XP_016866593.1:p.Arg1136Lys
XM_017011105.2:c.3377G>A	XP_016866594.1:p.Arg1126Lys
XM_017011106.2:c.3248G>A	XP_016866595.1:p.Arg1083Lys
XM_017011107.2:c.3227G>A	XP_016866596.1:p.Arg1076Lys
XR_002956289.1:n.3619G>A
NM_001363725.2:c.1076G>A	NP_001350654.1:p.Arg359Lys
NM_001371656.1:c.3455G>A	NP_001358585.1:p.Arg1152Lys
NM_001374820.1:c.3455G>A	NP_001361749.1:p.Arg1152Lys
NM_001374828.1:c.3575G>A MANE Select	NP_001361757.1:p.Arg1192Lys
NM_017519.3:c.3416G>A	NP_059989.3:p.Arg1139Lys