Canonical Allele Identifier: CA366389464

Gene: ARID1B

Linked Data

• dbSNP Id: rs879253747
• MyVariant Identifiers: chr6:g.157488235C>G (hg19) ; chr6:g.157167101C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157167101C>G , CM000668.2:g.157167101C>G	GRCh38
NC_000006.11:g.157488235C>G , CM000668.1:g.157488235C>G	GRCh37
NC_000006.10:g.157529927C>G	NCBI36
NG_032093.1:g.394172C>G
NG_032093.2:g.394172C>G
NG_066624.1:g.396076C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3151C>G	ENSP00000055163.8:p.Gln1051Glu
ENST00000414678.8:c.3061C>G	ENSP00000412835.3:p.Gln1021Glu
ENST00000637015.2:c.3280C>G	ENSP00000489729.2:p.Gln1094Glu
ENST00000319584.11:c.1165C>G	ENSP00000313006.7:p.Gln389Glu
ENST00000346085.10:c.3190C>G	ENSP00000344546.5:p.Gln1064Glu
ENST00000350026.10:c.2902C>G	ENSP00000055163.7:p.Gln968Glu
ENST00000414678.7:c.1309C>G	ENSP00000412835.2:p.Gln437Glu
ENST00000635849.1:c.472C>G	ENSP00000490948.1:p.Gln158Glu
ENST00000635957.1:c.106C>G	ENSP00000490385.1:p.Gln36Glu
ENST00000636426.1:n.315C>G
ENST00000636930.2:c.3151C>G MANE Select	ENSP00000490491.2:p.Gln1051Glu
ENST00000637015.1:c.519C>G
ENST00000637568.1:c.433C>G
ENST00000637722.1:n.1087C>G
ENST00000637810.1:c.652C>G	ENSP00000489636.1:p.Gln218Glu
ENST00000637904.1:c.652C>G	ENSP00000490550.1:p.Gln218Glu
ENST00000647938.1:c.2941C>G	ENSP00000498155.1:p.Gln981Glu
ENST00000319584.10:c.1168C>G	ENSP00000313006.6:p.Gln390Glu
ENST00000346085.9:c.2941C>G	ENSP00000344546.4:p.Gln981Glu
ENST00000350026.9:c.2902C>G	ENSP00000055163.7:p.Gln968Glu
ENST00000400790.3:c.103C>G	ENSP00000383596.3:p.Gln35Glu
ENST00000414678.6:c.1309C>G	ENSP00000412835.2:p.Gln437Glu
ENST00000478761.3:c.353C>G
NM_017519.2:c.2902C>G	NP_059989.2:p.Gln968Glu
NM_020732.3:c.2941C>G	NP_065783.3:p.Gln981Glu
XM_005267069.3:c.2902C>G	XP_005267126.2:p.Gln968Glu
XM_011535984.1:c.1981C>G	XP_011534286.1:p.Gln661Glu
XM_011535985.1:c.1801C>G	XP_011534287.1:p.Gln601Glu
XM_011535986.1:c.1561C>G	XP_011534288.1:p.Gln521Glu
XM_011535987.1:c.1180C>G	XP_011534289.1:p.Gln394Glu
XM_011535988.1:c.43C>G	XP_011534290.1:p.Gln15Glu
NM_001346813.1:c.2902C>G	NP_001333742.1:p.Gln968Glu
NM_001363725.1:c.652C>G	NP_001350654.1:p.Gln218Glu
XM_011535984.2:c.3112C>G	XP_011534286.2:p.Gln1038Glu
XM_011535988.3:c.43C>G	XP_011534290.1:p.Gln15Glu
XM_017011103.2:c.3013C>G	XP_016866592.1:p.Gln1005Glu
XM_017011104.1:c.2983C>G	XP_016866593.1:p.Gln995Glu
XM_017011105.2:c.3112C>G	XP_016866594.1:p.Gln1038Glu
XM_017011106.2:c.2983C>G	XP_016866595.1:p.Gln995Glu
XM_017011107.2:c.2803C>G	XP_016866596.1:p.Gln935Glu
XR_002956289.1:n.3195C>G
NM_001363725.2:c.652C>G	NP_001350654.1:p.Gln218Glu
NM_001371656.1:c.3190C>G	NP_001358585.1:p.Gln1064Glu
NM_001374820.1:c.3190C>G	NP_001361749.1:p.Gln1064Glu
NM_001374828.1:c.3151C>G MANE Select	NP_001361757.1:p.Gln1051Glu
NM_017519.3:c.3151C>G	NP_059989.3:p.Gln1051Glu