Canonical Allele Identifier: CA366227343

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316882
• COSMIC: COSM6316546 ; COSM6316547
• MyVariant Identifiers: chr6:g.157502157G>T (hg19) ; chr6:g.157181023G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181023G>T , CM000668.2:g.157181023G>T	GRCh38
NC_000006.11:g.157502157G>T , CM000668.1:g.157502157G>T	GRCh37
NC_000006.10:g.157543849G>T	NCBI36
NG_032093.1:g.408094G>T
NG_032093.2:g.408094G>T
NG_066624.1:g.409998G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3400G>T	ENSP00000055163.8:p.Gly1134Trp
ENST00000414678.8:c.3469G>T	ENSP00000412835.3:p.Gly1157Trp
ENST00000637015.2:c.3688G>T	ENSP00000489729.2:p.Gly1230Trp
ENST00000319584.11:c.1573G>T	ENSP00000313006.7:p.Gly525Trp
ENST00000346085.10:c.3439G>T	ENSP00000344546.5:p.Gly1147Trp
ENST00000350026.10:c.3151G>T	ENSP00000055163.7:p.Gly1051Trp
ENST00000414678.7:c.1717G>T	ENSP00000412835.2:p.Gly573Trp
ENST00000635849.1:c.880G>T	ENSP00000490948.1:p.Gly294Trp
ENST00000635957.1:c.514G>T	ENSP00000490385.1:p.Gly172Trp
ENST00000636930.2:c.3559G>T MANE Select	ENSP00000490491.2:p.Gly1187Trp
ENST00000636940.1:n.1556G>T
ENST00000637015.1:c.927G>T
ENST00000637568.1:c.841G>T
ENST00000637741.1:n.225G>T
ENST00000637810.1:c.901G>T	ENSP00000489636.1:p.Gly301Trp
ENST00000637904.1:c.1060G>T	ENSP00000490550.1:p.Gly354Trp
ENST00000647938.1:c.3190G>T	ENSP00000498155.1:p.Gly1064Trp
ENST00000319584.10:c.1576G>T	ENSP00000313006.6:p.Gly526Trp
ENST00000346085.9:c.3190G>T	ENSP00000344546.4:p.Gly1064Trp
ENST00000350026.9:c.3151G>T	ENSP00000055163.7:p.Gly1051Trp
ENST00000400790.3:c.352G>T	ENSP00000383596.3:p.Gly118Trp
ENST00000414678.6:c.1717G>T	ENSP00000412835.2:p.Gly573Trp
ENST00000478761.3:c.761G>T
NM_017519.2:c.3151G>T	NP_059989.2:p.Gly1051Trp
NM_020732.3:c.3190G>T	NP_065783.3:p.Gly1064Trp
XM_005267069.3:c.3310G>T	XP_005267126.2:p.Gly1104Trp
XM_011535984.1:c.2389G>T	XP_011534286.1:p.Gly797Trp
XM_011535985.1:c.2209G>T	XP_011534287.1:p.Gly737Trp
XM_011535986.1:c.1969G>T	XP_011534288.1:p.Gly657Trp
XM_011535987.1:c.1588G>T	XP_011534289.1:p.Gly530Trp
XM_011535988.1:c.451G>T	XP_011534290.1:p.Gly151Trp
NM_001346813.1:c.3310G>T	NP_001333742.1:p.Gly1104Trp
NM_001363725.1:c.1060G>T	NP_001350654.1:p.Gly354Trp
XM_011535984.2:c.3520G>T	XP_011534286.2:p.Gly1174Trp
XM_011535988.3:c.451G>T	XP_011534290.1:p.Gly151Trp
XM_017011103.2:c.3421G>T	XP_016866592.1:p.Gly1141Trp
XM_017011104.1:c.3391G>T	XP_016866593.1:p.Gly1131Trp
XM_017011105.2:c.3361G>T	XP_016866594.1:p.Gly1121Trp
XM_017011106.2:c.3232G>T	XP_016866595.1:p.Gly1078Trp
XM_017011107.2:c.3211G>T	XP_016866596.1:p.Gly1071Trp
XR_002956289.1:n.3603G>T
NM_001363725.2:c.1060G>T	NP_001350654.1:p.Gly354Trp
NM_001371656.1:c.3439G>T	NP_001358585.1:p.Gly1147Trp
NM_001374820.1:c.3439G>T	NP_001361749.1:p.Gly1147Trp
NM_001374828.1:c.3559G>T MANE Select	NP_001361757.1:p.Gly1187Trp
NM_017519.3:c.3400G>T	NP_059989.3:p.Gly1134Trp