Canonical Allele Identifier: CA366228214

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317589
• MyVariant Identifiers: chr6:g.157502264C>G (hg19) ; chr6:g.157181130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181130C>G , CM000668.2:g.157181130C>G	GRCh38
NC_000006.11:g.157502264C>G , CM000668.1:g.157502264C>G	GRCh37
NC_000006.10:g.157543956C>G	NCBI36
NG_032093.1:g.408201C>G
NG_032093.2:g.408201C>G
NG_066624.1:g.410105C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3507C>G	ENSP00000055163.8:p.Asp1169Glu
ENST00000414678.8:c.3576C>G	ENSP00000412835.3:p.Asp1192Glu
ENST00000637015.2:c.3795C>G	ENSP00000489729.2:p.Asp1265Glu
ENST00000319584.11:c.1680C>G	ENSP00000313006.7:p.Asp560Glu
ENST00000346085.10:c.3546C>G	ENSP00000344546.5:p.Asp1182Glu
ENST00000350026.10:c.3258C>G	ENSP00000055163.7:p.Asp1086Glu
ENST00000414678.7:c.1824C>G	ENSP00000412835.2:p.Asp608Glu
ENST00000635849.1:c.987C>G	ENSP00000490948.1:p.Asp329Glu
ENST00000635957.1:c.621C>G	ENSP00000490385.1:p.Asp207Glu
ENST00000636930.2:c.3666C>G MANE Select	ENSP00000490491.2:p.Asp1222Glu
ENST00000636940.1:n.1663C>G
ENST00000637015.1:c.1034C>G
ENST00000637568.1:c.948C>G
ENST00000637741.1:n.332C>G
ENST00000637810.1:c.1008C>G	ENSP00000489636.1:p.Asp336Glu
ENST00000637904.1:c.1167C>G	ENSP00000490550.1:p.Asp389Glu
ENST00000647938.1:c.3297C>G	ENSP00000498155.1:p.Asp1099Glu
ENST00000319584.10:c.1683C>G	ENSP00000313006.6:p.Asp561Glu
ENST00000346085.9:c.3297C>G	ENSP00000344546.4:p.Asp1099Glu
ENST00000350026.9:c.3258C>G	ENSP00000055163.7:p.Asp1086Glu
ENST00000400790.3:c.459C>G	ENSP00000383596.3:p.Asp153Glu
ENST00000414678.6:c.1824C>G	ENSP00000412835.2:p.Asp608Glu
ENST00000478761.3:c.868C>G
NM_017519.2:c.3258C>G	NP_059989.2:p.Asp1086Glu
NM_020732.3:c.3297C>G	NP_065783.3:p.Asp1099Glu
XM_005267069.3:c.3417C>G	XP_005267126.2:p.Asp1139Glu
XM_011535984.1:c.2496C>G	XP_011534286.1:p.Asp832Glu
XM_011535985.1:c.2316C>G	XP_011534287.1:p.Asp772Glu
XM_011535986.1:c.2076C>G	XP_011534288.1:p.Asp692Glu
XM_011535987.1:c.1695C>G	XP_011534289.1:p.Asp565Glu
XM_011535988.1:c.558C>G	XP_011534290.1:p.Asp186Glu
NM_001346813.1:c.3417C>G	NP_001333742.1:p.Asp1139Glu
NM_001363725.1:c.1167C>G	NP_001350654.1:p.Asp389Glu
XM_011535984.2:c.3627C>G	XP_011534286.2:p.Asp1209Glu
XM_011535988.3:c.558C>G	XP_011534290.1:p.Asp186Glu
XM_017011103.2:c.3528C>G	XP_016866592.1:p.Asp1176Glu
XM_017011104.1:c.3498C>G	XP_016866593.1:p.Asp1166Glu
XM_017011105.2:c.3468C>G	XP_016866594.1:p.Asp1156Glu
XM_017011106.2:c.3339C>G	XP_016866595.1:p.Asp1113Glu
XM_017011107.2:c.3318C>G	XP_016866596.1:p.Asp1106Glu
XR_002956289.1:n.3710C>G
NM_001363725.2:c.1167C>G	NP_001350654.1:p.Asp389Glu
NM_001371656.1:c.3546C>G	NP_001358585.1:p.Asp1182Glu
NM_001374820.1:c.3546C>G	NP_001361749.1:p.Asp1182Glu
NM_001374828.1:c.3666C>G MANE Select	NP_001361757.1:p.Asp1222Glu
NM_017519.3:c.3507C>G	NP_059989.3:p.Asp1169Glu