Canonical Allele Identifier: CA366227598

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317094
• MyVariant Identifiers: chr6:g.157502188A>G (hg19) ; chr6:g.157181054A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181054A>G , CM000668.2:g.157181054A>G	GRCh38
NC_000006.11:g.157502188A>G , CM000668.1:g.157502188A>G	GRCh37
NC_000006.10:g.157543880A>G	NCBI36
NG_032093.1:g.408125A>G
NG_032093.2:g.408125A>G
NG_066624.1:g.410029A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3431A>G	ENSP00000055163.8:p.Asp1144Gly
ENST00000414678.8:c.3500A>G	ENSP00000412835.3:p.Asp1167Gly
ENST00000637015.2:c.3719A>G	ENSP00000489729.2:p.Asp1240Gly
ENST00000319584.11:c.1604A>G	ENSP00000313006.7:p.Asp535Gly
ENST00000346085.10:c.3470A>G	ENSP00000344546.5:p.Asp1157Gly
ENST00000350026.10:c.3182A>G	ENSP00000055163.7:p.Asp1061Gly
ENST00000414678.7:c.1748A>G	ENSP00000412835.2:p.Asp583Gly
ENST00000635849.1:c.911A>G	ENSP00000490948.1:p.Asp304Gly
ENST00000635957.1:c.545A>G	ENSP00000490385.1:p.Asp182Gly
ENST00000636930.2:c.3590A>G MANE Select	ENSP00000490491.2:p.Asp1197Gly
ENST00000636940.1:n.1587A>G
ENST00000637015.1:c.958A>G
ENST00000637568.1:c.872A>G
ENST00000637741.1:n.256A>G
ENST00000637810.1:c.932A>G	ENSP00000489636.1:p.Asp311Gly
ENST00000637904.1:c.1091A>G	ENSP00000490550.1:p.Asp364Gly
ENST00000647938.1:c.3221A>G	ENSP00000498155.1:p.Asp1074Gly
ENST00000319584.10:c.1607A>G	ENSP00000313006.6:p.Asp536Gly
ENST00000346085.9:c.3221A>G	ENSP00000344546.4:p.Asp1074Gly
ENST00000350026.9:c.3182A>G	ENSP00000055163.7:p.Asp1061Gly
ENST00000400790.3:c.383A>G	ENSP00000383596.3:p.Asp128Gly
ENST00000414678.6:c.1748A>G	ENSP00000412835.2:p.Asp583Gly
ENST00000478761.3:c.792A>G
NM_017519.2:c.3182A>G	NP_059989.2:p.Asp1061Gly
NM_020732.3:c.3221A>G	NP_065783.3:p.Asp1074Gly
XM_005267069.3:c.3341A>G	XP_005267126.2:p.Asp1114Gly
XM_011535984.1:c.2420A>G	XP_011534286.1:p.Asp807Gly
XM_011535985.1:c.2240A>G	XP_011534287.1:p.Asp747Gly
XM_011535986.1:c.2000A>G	XP_011534288.1:p.Asp667Gly
XM_011535987.1:c.1619A>G	XP_011534289.1:p.Asp540Gly
XM_011535988.1:c.482A>G	XP_011534290.1:p.Asp161Gly
NM_001346813.1:c.3341A>G	NP_001333742.1:p.Asp1114Gly
NM_001363725.1:c.1091A>G	NP_001350654.1:p.Asp364Gly
XM_011535984.2:c.3551A>G	XP_011534286.2:p.Asp1184Gly
XM_011535988.3:c.482A>G	XP_011534290.1:p.Asp161Gly
XM_017011103.2:c.3452A>G	XP_016866592.1:p.Asp1151Gly
XM_017011104.1:c.3422A>G	XP_016866593.1:p.Asp1141Gly
XM_017011105.2:c.3392A>G	XP_016866594.1:p.Asp1131Gly
XM_017011106.2:c.3263A>G	XP_016866595.1:p.Asp1088Gly
XM_017011107.2:c.3242A>G	XP_016866596.1:p.Asp1081Gly
XR_002956289.1:n.3634A>G
NM_001363725.2:c.1091A>G	NP_001350654.1:p.Asp364Gly
NM_001371656.1:c.3470A>G	NP_001358585.1:p.Asp1157Gly
NM_001374820.1:c.3470A>G	NP_001361749.1:p.Asp1157Gly
NM_001374828.1:c.3590A>G MANE Select	NP_001361757.1:p.Asp1197Gly
NM_017519.3:c.3431A>G	NP_059989.3:p.Asp1144Gly