Canonical Allele Identifier: CA366227354

Gene: ARID1B

Linked Data

• dbSNP Id: rs771373121
• MyVariant Identifiers: chr6:g.157502158G>T (hg19) ; chr6:g.157181024G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181024G>T , CM000668.2:g.157181024G>T	GRCh38
NC_000006.11:g.157502158G>T , CM000668.1:g.157502158G>T	GRCh37
NC_000006.10:g.157543850G>T	NCBI36
NG_032093.1:g.408095G>T
NG_032093.2:g.408095G>T
NG_066624.1:g.409999G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3401G>T	ENSP00000055163.8:p.Gly1134Val
ENST00000414678.8:c.3470G>T	ENSP00000412835.3:p.Gly1157Val
ENST00000637015.2:c.3689G>T	ENSP00000489729.2:p.Gly1230Val
ENST00000319584.11:c.1574G>T	ENSP00000313006.7:p.Gly525Val
ENST00000346085.10:c.3440G>T	ENSP00000344546.5:p.Gly1147Val
ENST00000350026.10:c.3152G>T	ENSP00000055163.7:p.Gly1051Val
ENST00000414678.7:c.1718G>T	ENSP00000412835.2:p.Gly573Val
ENST00000635849.1:c.881G>T	ENSP00000490948.1:p.Gly294Val
ENST00000635957.1:c.515G>T	ENSP00000490385.1:p.Gly172Val
ENST00000636930.2:c.3560G>T MANE Select	ENSP00000490491.2:p.Gly1187Val
ENST00000636940.1:n.1557G>T
ENST00000637015.1:c.928G>T
ENST00000637568.1:c.842G>T
ENST00000637741.1:n.226G>T
ENST00000637810.1:c.902G>T	ENSP00000489636.1:p.Gly301Val
ENST00000637904.1:c.1061G>T	ENSP00000490550.1:p.Gly354Val
ENST00000647938.1:c.3191G>T	ENSP00000498155.1:p.Gly1064Val
ENST00000319584.10:c.1577G>T	ENSP00000313006.6:p.Gly526Val
ENST00000346085.9:c.3191G>T	ENSP00000344546.4:p.Gly1064Val
ENST00000350026.9:c.3152G>T	ENSP00000055163.7:p.Gly1051Val
ENST00000400790.3:c.353G>T	ENSP00000383596.3:p.Gly118Val
ENST00000414678.6:c.1718G>T	ENSP00000412835.2:p.Gly573Val
ENST00000478761.3:c.762G>T
NM_017519.2:c.3152G>T	NP_059989.2:p.Gly1051Val
NM_020732.3:c.3191G>T	NP_065783.3:p.Gly1064Val
XM_005267069.3:c.3311G>T	XP_005267126.2:p.Gly1104Val
XM_011535984.1:c.2390G>T	XP_011534286.1:p.Gly797Val
XM_011535985.1:c.2210G>T	XP_011534287.1:p.Gly737Val
XM_011535986.1:c.1970G>T	XP_011534288.1:p.Gly657Val
XM_011535987.1:c.1589G>T	XP_011534289.1:p.Gly530Val
XM_011535988.1:c.452G>T	XP_011534290.1:p.Gly151Val
NM_001346813.1:c.3311G>T	NP_001333742.1:p.Gly1104Val
NM_001363725.1:c.1061G>T	NP_001350654.1:p.Gly354Val
XM_011535984.2:c.3521G>T	XP_011534286.2:p.Gly1174Val
XM_011535988.3:c.452G>T	XP_011534290.1:p.Gly151Val
XM_017011103.2:c.3422G>T	XP_016866592.1:p.Gly1141Val
XM_017011104.1:c.3392G>T	XP_016866593.1:p.Gly1131Val
XM_017011105.2:c.3362G>T	XP_016866594.1:p.Gly1121Val
XM_017011106.2:c.3233G>T	XP_016866595.1:p.Gly1078Val
XM_017011107.2:c.3212G>T	XP_016866596.1:p.Gly1071Val
XR_002956289.1:n.3604G>T
NM_001363725.2:c.1061G>T	NP_001350654.1:p.Gly354Val
NM_001371656.1:c.3440G>T	NP_001358585.1:p.Gly1147Val
NM_001374820.1:c.3440G>T	NP_001361749.1:p.Gly1147Val
NM_001374828.1:c.3560G>T MANE Select	NP_001361757.1:p.Gly1187Val
NM_017519.3:c.3401G>T	NP_059989.3:p.Gly1134Val