Canonical Allele Identifier: CA366227860

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502212A>G (hg19) ; chr6:g.157181078A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181078A>G , CM000668.2:g.157181078A>G	GRCh38
NC_000006.11:g.157502212A>G , CM000668.1:g.157502212A>G	GRCh37
NC_000006.10:g.157543904A>G	NCBI36
NG_032093.1:g.408149A>G
NG_032093.2:g.408149A>G
NG_066624.1:g.410053A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3455A>G	ENSP00000055163.8:p.Glu1152Gly
ENST00000414678.8:c.3524A>G	ENSP00000412835.3:p.Glu1175Gly
ENST00000637015.2:c.3743A>G	ENSP00000489729.2:p.Glu1248Gly
ENST00000319584.11:c.1628A>G	ENSP00000313006.7:p.Glu543Gly
ENST00000346085.10:c.3494A>G	ENSP00000344546.5:p.Glu1165Gly
ENST00000350026.10:c.3206A>G	ENSP00000055163.7:p.Glu1069Gly
ENST00000414678.7:c.1772A>G	ENSP00000412835.2:p.Glu591Gly
ENST00000635849.1:c.935A>G	ENSP00000490948.1:p.Glu312Gly
ENST00000635957.1:c.569A>G	ENSP00000490385.1:p.Glu190Gly
ENST00000636930.2:c.3614A>G MANE Select	ENSP00000490491.2:p.Glu1205Gly
ENST00000636940.1:n.1611A>G
ENST00000637015.1:c.982A>G
ENST00000637568.1:c.896A>G
ENST00000637741.1:n.280A>G
ENST00000637810.1:c.956A>G	ENSP00000489636.1:p.Glu319Gly
ENST00000637904.1:c.1115A>G	ENSP00000490550.1:p.Glu372Gly
ENST00000647938.1:c.3245A>G	ENSP00000498155.1:p.Glu1082Gly
ENST00000319584.10:c.1631A>G	ENSP00000313006.6:p.Glu544Gly
ENST00000346085.9:c.3245A>G	ENSP00000344546.4:p.Glu1082Gly
ENST00000350026.9:c.3206A>G	ENSP00000055163.7:p.Glu1069Gly
ENST00000400790.3:c.407A>G	ENSP00000383596.3:p.Glu136Gly
ENST00000414678.6:c.1772A>G	ENSP00000412835.2:p.Glu591Gly
ENST00000478761.3:c.816A>G
NM_017519.2:c.3206A>G	NP_059989.2:p.Glu1069Gly
NM_020732.3:c.3245A>G	NP_065783.3:p.Glu1082Gly
XM_005267069.3:c.3365A>G	XP_005267126.2:p.Glu1122Gly
XM_011535984.1:c.2444A>G	XP_011534286.1:p.Glu815Gly
XM_011535985.1:c.2264A>G	XP_011534287.1:p.Glu755Gly
XM_011535986.1:c.2024A>G	XP_011534288.1:p.Glu675Gly
XM_011535987.1:c.1643A>G	XP_011534289.1:p.Glu548Gly
XM_011535988.1:c.506A>G	XP_011534290.1:p.Glu169Gly
NM_001346813.1:c.3365A>G	NP_001333742.1:p.Glu1122Gly
NM_001363725.1:c.1115A>G	NP_001350654.1:p.Glu372Gly
XM_011535984.2:c.3575A>G	XP_011534286.2:p.Glu1192Gly
XM_011535988.3:c.506A>G	XP_011534290.1:p.Glu169Gly
XM_017011103.2:c.3476A>G	XP_016866592.1:p.Glu1159Gly
XM_017011104.1:c.3446A>G	XP_016866593.1:p.Glu1149Gly
XM_017011105.2:c.3416A>G	XP_016866594.1:p.Glu1139Gly
XM_017011106.2:c.3287A>G	XP_016866595.1:p.Glu1096Gly
XM_017011107.2:c.3266A>G	XP_016866596.1:p.Glu1089Gly
XR_002956289.1:n.3658A>G
NM_001363725.2:c.1115A>G	NP_001350654.1:p.Glu372Gly
NM_001371656.1:c.3494A>G	NP_001358585.1:p.Glu1165Gly
NM_001374820.1:c.3494A>G	NP_001361749.1:p.Glu1165Gly
NM_001374828.1:c.3614A>G MANE Select	NP_001361757.1:p.Glu1205Gly
NM_017519.3:c.3455A>G	NP_059989.3:p.Glu1152Gly