Canonical Allele Identifier: CA366228210

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231259
• MyVariant Identifiers: chr6:g.157502263A>G (hg19) ; chr6:g.157181129A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181129A>G , CM000668.2:g.157181129A>G	GRCh38
NC_000006.11:g.157502263A>G , CM000668.1:g.157502263A>G	GRCh37
NC_000006.10:g.157543955A>G	NCBI36
NG_032093.1:g.408200A>G
NG_032093.2:g.408200A>G
NG_066624.1:g.410104A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3506A>G	ENSP00000055163.8:p.Asp1169Gly
ENST00000414678.8:c.3575A>G	ENSP00000412835.3:p.Asp1192Gly
ENST00000637015.2:c.3794A>G	ENSP00000489729.2:p.Asp1265Gly
ENST00000319584.11:c.1679A>G	ENSP00000313006.7:p.Asp560Gly
ENST00000346085.10:c.3545A>G	ENSP00000344546.5:p.Asp1182Gly
ENST00000350026.10:c.3257A>G	ENSP00000055163.7:p.Asp1086Gly
ENST00000414678.7:c.1823A>G	ENSP00000412835.2:p.Asp608Gly
ENST00000635849.1:c.986A>G	ENSP00000490948.1:p.Asp329Gly
ENST00000635957.1:c.620A>G	ENSP00000490385.1:p.Asp207Gly
ENST00000636930.2:c.3665A>G MANE Select	ENSP00000490491.2:p.Asp1222Gly
ENST00000636940.1:n.1662A>G
ENST00000637015.1:c.1033A>G
ENST00000637568.1:c.947A>G
ENST00000637741.1:n.331A>G
ENST00000637810.1:c.1007A>G	ENSP00000489636.1:p.Asp336Gly
ENST00000637904.1:c.1166A>G	ENSP00000490550.1:p.Asp389Gly
ENST00000647938.1:c.3296A>G	ENSP00000498155.1:p.Asp1099Gly
ENST00000319584.10:c.1682A>G	ENSP00000313006.6:p.Asp561Gly
ENST00000346085.9:c.3296A>G	ENSP00000344546.4:p.Asp1099Gly
ENST00000350026.9:c.3257A>G	ENSP00000055163.7:p.Asp1086Gly
ENST00000400790.3:c.458A>G	ENSP00000383596.3:p.Asp153Gly
ENST00000414678.6:c.1823A>G	ENSP00000412835.2:p.Asp608Gly
ENST00000478761.3:c.867A>G
NM_017519.2:c.3257A>G	NP_059989.2:p.Asp1086Gly
NM_020732.3:c.3296A>G	NP_065783.3:p.Asp1099Gly
XM_005267069.3:c.3416A>G	XP_005267126.2:p.Asp1139Gly
XM_011535984.1:c.2495A>G	XP_011534286.1:p.Asp832Gly
XM_011535985.1:c.2315A>G	XP_011534287.1:p.Asp772Gly
XM_011535986.1:c.2075A>G	XP_011534288.1:p.Asp692Gly
XM_011535987.1:c.1694A>G	XP_011534289.1:p.Asp565Gly
XM_011535988.1:c.557A>G	XP_011534290.1:p.Asp186Gly
NM_001346813.1:c.3416A>G	NP_001333742.1:p.Asp1139Gly
NM_001363725.1:c.1166A>G	NP_001350654.1:p.Asp389Gly
XM_011535984.2:c.3626A>G	XP_011534286.2:p.Asp1209Gly
XM_011535988.3:c.557A>G	XP_011534290.1:p.Asp186Gly
XM_017011103.2:c.3527A>G	XP_016866592.1:p.Asp1176Gly
XM_017011104.1:c.3497A>G	XP_016866593.1:p.Asp1166Gly
XM_017011105.2:c.3467A>G	XP_016866594.1:p.Asp1156Gly
XM_017011106.2:c.3338A>G	XP_016866595.1:p.Asp1113Gly
XM_017011107.2:c.3317A>G	XP_016866596.1:p.Asp1106Gly
XR_002956289.1:n.3709A>G
NM_001363725.2:c.1166A>G	NP_001350654.1:p.Asp389Gly
NM_001371656.1:c.3545A>G	NP_001358585.1:p.Asp1182Gly
NM_001374820.1:c.3545A>G	NP_001361749.1:p.Asp1182Gly
NM_001374828.1:c.3665A>G MANE Select	NP_001361757.1:p.Asp1222Gly
NM_017519.3:c.3506A>G	NP_059989.3:p.Asp1169Gly