Canonical Allele Identifier: CA366239622

Gene: ARID1B

Linked Data

• dbSNP Id: rs1163916797
• gnomAD v3: 6-157198839-G-A
• gnomAD v4: 6-157198839-G-A
• MyVariant Identifiers: chr6:g.157519973G>A (hg19) ; chr6:g.157198839G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198839G>A , CM000668.2:g.157198839G>A	GRCh38
NC_000006.11:g.157519973G>A , CM000668.1:g.157519973G>A	GRCh37
NC_000006.10:g.157561665G>A	NCBI36
NG_032093.1:g.425910G>A
NG_032093.2:g.425910G>A
NG_066624.1:g.427814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4252G>A	ENSP00000055163.8:p.Gly1418Ser
ENST00000414678.8:c.4321G>A	ENSP00000412835.3:p.Gly1441Ser
ENST00000637015.2:c.4540G>A	ENSP00000489729.2:p.Gly1514Ser
ENST00000346085.10:c.4291G>A	ENSP00000344546.5:p.Gly1431Ser
ENST00000350026.10:c.4003G>A	ENSP00000055163.7:p.Gly1335Ser
ENST00000414678.7:c.2569G>A	ENSP00000412835.2:p.Gly857Ser
ENST00000635849.1:c.1732G>A	ENSP00000490948.1:p.Gly578Ser
ENST00000635957.1:c.1363G>A	ENSP00000490385.1:p.Gly455Ser
ENST00000636227.1:n.2874G>A
ENST00000636254.1:n.331G>A
ENST00000636930.2:c.4411G>A MANE Select	ENSP00000490491.2:p.Gly1471Ser
ENST00000636940.1:n.2408G>A
ENST00000637015.1:c.1779G>A
ENST00000637568.1:c.1693G>A
ENST00000637741.1:n.1077G>A
ENST00000637810.1:c.1753G>A	ENSP00000489636.1:p.Gly585Ser
ENST00000637904.1:c.1912G>A	ENSP00000490550.1:p.Gly638Ser
ENST00000647938.1:c.4042G>A	ENSP00000498155.1:p.Gly1348Ser
ENST00000346085.9:c.4042G>A	ENSP00000344546.4:p.Gly1348Ser
ENST00000350026.9:c.4003G>A	ENSP00000055163.7:p.Gly1335Ser
ENST00000414678.6:c.2569G>A	ENSP00000412835.2:p.Gly857Ser
NM_017519.2:c.4003G>A	NP_059989.2:p.Gly1335Ser
NM_020732.3:c.4042G>A	NP_065783.3:p.Gly1348Ser
XM_005267069.3:c.4162G>A	XP_005267126.2:p.Gly1388Ser
XM_011535984.1:c.3241G>A	XP_011534286.1:p.Gly1081Ser
XM_011535985.1:c.3061G>A	XP_011534287.1:p.Gly1021Ser
XM_011535986.1:c.2821G>A	XP_011534288.1:p.Gly941Ser
XM_011535987.1:c.2440G>A	XP_011534289.1:p.Gly814Ser
XM_011535988.1:c.1303G>A	XP_011534290.1:p.Gly435Ser
NM_001346813.1:c.4162G>A	NP_001333742.1:p.Gly1388Ser
NM_001363725.1:c.1912G>A	NP_001350654.1:p.Gly638Ser
XM_011535984.2:c.4372G>A	XP_011534286.2:p.Gly1458Ser
XM_011535988.3:c.1303G>A	XP_011534290.1:p.Gly435Ser
XM_017011103.2:c.4273G>A	XP_016866592.1:p.Gly1425Ser
XM_017011104.1:c.4243G>A	XP_016866593.1:p.Gly1415Ser
XM_017011105.2:c.4213G>A	XP_016866594.1:p.Gly1405Ser
XM_017011106.2:c.4084G>A	XP_016866595.1:p.Gly1362Ser
XM_017011107.2:c.4063G>A	XP_016866596.1:p.Gly1355Ser
XR_002956289.1:n.4427-1866G>A
NM_001363725.2:c.1912G>A	NP_001350654.1:p.Gly638Ser
NM_001371656.1:c.4291G>A	NP_001358585.1:p.Gly1431Ser
NM_001374820.1:c.4291G>A	NP_001361749.1:p.Gly1431Ser
NM_001374828.1:c.4411G>A MANE Select	NP_001361757.1:p.Gly1471Ser
NM_017519.3:c.4252G>A	NP_059989.3:p.Gly1418Ser