Canonical Allele Identifier: CA366239630

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366109
• gnomAD v4: 6-157198840-G-A
• MyVariant Identifiers: chr6:g.157519974G>A (hg19) ; chr6:g.157198840G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198840G>A , CM000668.2:g.157198840G>A	GRCh38
NC_000006.11:g.157519974G>A , CM000668.1:g.157519974G>A	GRCh37
NC_000006.10:g.157561666G>A	NCBI36
NG_032093.1:g.425911G>A
NG_032093.2:g.425911G>A
NG_066624.1:g.427815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4253G>A	ENSP00000055163.8:p.Gly1418Asp
ENST00000414678.8:c.4322G>A	ENSP00000412835.3:p.Gly1441Asp
ENST00000637015.2:c.4541G>A	ENSP00000489729.2:p.Gly1514Asp
ENST00000346085.10:c.4292G>A	ENSP00000344546.5:p.Gly1431Asp
ENST00000350026.10:c.4004G>A	ENSP00000055163.7:p.Gly1335Asp
ENST00000414678.7:c.2570G>A	ENSP00000412835.2:p.Gly857Asp
ENST00000635849.1:c.1733G>A	ENSP00000490948.1:p.Gly578Asp
ENST00000635957.1:c.1364G>A	ENSP00000490385.1:p.Gly455Asp
ENST00000636227.1:n.2875G>A
ENST00000636254.1:n.332G>A
ENST00000636930.2:c.4412G>A MANE Select	ENSP00000490491.2:p.Gly1471Asp
ENST00000636940.1:n.2409G>A
ENST00000637015.1:c.1780G>A
ENST00000637568.1:c.1694G>A
ENST00000637741.1:n.1078G>A
ENST00000637810.1:c.1754G>A	ENSP00000489636.1:p.Gly585Asp
ENST00000637904.1:c.1913G>A	ENSP00000490550.1:p.Gly638Asp
ENST00000647938.1:c.4043G>A	ENSP00000498155.1:p.Gly1348Asp
ENST00000346085.9:c.4043G>A	ENSP00000344546.4:p.Gly1348Asp
ENST00000350026.9:c.4004G>A	ENSP00000055163.7:p.Gly1335Asp
ENST00000414678.6:c.2570G>A	ENSP00000412835.2:p.Gly857Asp
NM_017519.2:c.4004G>A	NP_059989.2:p.Gly1335Asp
NM_020732.3:c.4043G>A	NP_065783.3:p.Gly1348Asp
XM_005267069.3:c.4163G>A	XP_005267126.2:p.Gly1388Asp
XM_011535984.1:c.3242G>A	XP_011534286.1:p.Gly1081Asp
XM_011535985.1:c.3062G>A	XP_011534287.1:p.Gly1021Asp
XM_011535986.1:c.2822G>A	XP_011534288.1:p.Gly941Asp
XM_011535987.1:c.2441G>A	XP_011534289.1:p.Gly814Asp
XM_011535988.1:c.1304G>A	XP_011534290.1:p.Gly435Asp
NM_001346813.1:c.4163G>A	NP_001333742.1:p.Gly1388Asp
NM_001363725.1:c.1913G>A	NP_001350654.1:p.Gly638Asp
XM_011535984.2:c.4373G>A	XP_011534286.2:p.Gly1458Asp
XM_011535988.3:c.1304G>A	XP_011534290.1:p.Gly435Asp
XM_017011103.2:c.4274G>A	XP_016866592.1:p.Gly1425Asp
XM_017011104.1:c.4244G>A	XP_016866593.1:p.Gly1415Asp
XM_017011105.2:c.4214G>A	XP_016866594.1:p.Gly1405Asp
XM_017011106.2:c.4085G>A	XP_016866595.1:p.Gly1362Asp
XM_017011107.2:c.4064G>A	XP_016866596.1:p.Gly1355Asp
XR_002956289.1:n.4427-1865G>A
NM_001363725.2:c.1913G>A	NP_001350654.1:p.Gly638Asp
NM_001371656.1:c.4292G>A	NP_001358585.1:p.Gly1431Asp
NM_001374820.1:c.4292G>A	NP_001361749.1:p.Gly1431Asp
NM_001374828.1:c.4412G>A MANE Select	NP_001361757.1:p.Gly1471Asp
NM_017519.3:c.4253G>A	NP_059989.3:p.Gly1418Asp