Canonical Allele Identifier: CA366227855

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317250
• MyVariant Identifiers: chr6:g.157502212A>T (hg19) ; chr6:g.157181078A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3455A>T	ENSP00000055163.8:p.Glu1152Val
ENST00000414678.8:c.3524A>T	ENSP00000412835.3:p.Glu1175Val
ENST00000637015.2:c.3743A>T	ENSP00000489729.2:p.Glu1248Val
ENST00000319584.11:c.1628A>T	ENSP00000313006.7:p.Glu543Val
ENST00000346085.10:c.3494A>T	ENSP00000344546.5:p.Glu1165Val
ENST00000350026.10:c.3206A>T	ENSP00000055163.7:p.Glu1069Val
ENST00000414678.7:c.1772A>T	ENSP00000412835.2:p.Glu591Val
ENST00000635849.1:c.935A>T	ENSP00000490948.1:p.Glu312Val
ENST00000635957.1:c.569A>T	ENSP00000490385.1:p.Glu190Val
ENST00000636930.2:c.3614A>T MANE Select	ENSP00000490491.2:p.Glu1205Val
ENST00000636940.1:n.1611A>T
ENST00000637015.1:c.982A>T
ENST00000637568.1:c.896A>T
ENST00000637741.1:n.280A>T
ENST00000637810.1:c.956A>T	ENSP00000489636.1:p.Glu319Val
ENST00000637904.1:c.1115A>T	ENSP00000490550.1:p.Glu372Val
ENST00000647938.1:c.3245A>T	ENSP00000498155.1:p.Glu1082Val
ENST00000319584.10:c.1631A>T	ENSP00000313006.6:p.Glu544Val
ENST00000346085.9:c.3245A>T	ENSP00000344546.4:p.Glu1082Val
ENST00000350026.9:c.3206A>T	ENSP00000055163.7:p.Glu1069Val
ENST00000400790.3:c.407A>T	ENSP00000383596.3:p.Glu136Val
ENST00000414678.6:c.1772A>T	ENSP00000412835.2:p.Glu591Val
ENST00000478761.3:c.816A>T
NM_017519.2:c.3206A>T	NP_059989.2:p.Glu1069Val
NM_020732.3:c.3245A>T	NP_065783.3:p.Glu1082Val
XM_005267069.3:c.3365A>T	XP_005267126.2:p.Glu1122Val
XM_011535984.1:c.2444A>T	XP_011534286.1:p.Glu815Val
XM_011535985.1:c.2264A>T	XP_011534287.1:p.Glu755Val
XM_011535986.1:c.2024A>T	XP_011534288.1:p.Glu675Val
XM_011535987.1:c.1643A>T	XP_011534289.1:p.Glu548Val
XM_011535988.1:c.506A>T	XP_011534290.1:p.Glu169Val
NM_001346813.1:c.3365A>T	NP_001333742.1:p.Glu1122Val
NM_001363725.1:c.1115A>T	NP_001350654.1:p.Glu372Val
XM_011535984.2:c.3575A>T	XP_011534286.2:p.Glu1192Val
XM_011535988.3:c.506A>T	XP_011534290.1:p.Glu169Val
XM_017011103.2:c.3476A>T	XP_016866592.1:p.Glu1159Val
XM_017011104.1:c.3446A>T	XP_016866593.1:p.Glu1149Val
XM_017011105.2:c.3416A>T	XP_016866594.1:p.Glu1139Val
XM_017011106.2:c.3287A>T	XP_016866595.1:p.Glu1096Val
XM_017011107.2:c.3266A>T	XP_016866596.1:p.Glu1089Val
XR_002956289.1:n.3658A>T
NM_001363725.2:c.1115A>T	NP_001350654.1:p.Glu372Val
NM_001371656.1:c.3494A>T	NP_001358585.1:p.Glu1165Val
NM_001374820.1:c.3494A>T	NP_001361749.1:p.Glu1165Val
NM_001374828.1:c.3614A>T MANE Select	NP_001361757.1:p.Glu1205Val
NM_017519.3:c.3455A>T	NP_059989.3:p.Glu1152Val