Canonical Allele Identifier: CA366227866

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3455A>C	ENSP00000055163.8:p.Glu1152Ala
ENST00000414678.8:c.3524A>C	ENSP00000412835.3:p.Glu1175Ala
ENST00000637015.2:c.3743A>C	ENSP00000489729.2:p.Glu1248Ala
ENST00000319584.11:c.1628A>C	ENSP00000313006.7:p.Glu543Ala
ENST00000346085.10:c.3494A>C	ENSP00000344546.5:p.Glu1165Ala
ENST00000350026.10:c.3206A>C	ENSP00000055163.7:p.Glu1069Ala
ENST00000414678.7:c.1772A>C	ENSP00000412835.2:p.Glu591Ala
ENST00000635849.1:c.935A>C	ENSP00000490948.1:p.Glu312Ala
ENST00000635957.1:c.569A>C	ENSP00000490385.1:p.Glu190Ala
ENST00000636930.2:c.3614A>C MANE Select	ENSP00000490491.2:p.Glu1205Ala
ENST00000636940.1:n.1611A>C
ENST00000637015.1:c.982A>C
ENST00000637568.1:c.896A>C
ENST00000637741.1:n.280A>C
ENST00000637810.1:c.956A>C	ENSP00000489636.1:p.Glu319Ala
ENST00000637904.1:c.1115A>C	ENSP00000490550.1:p.Glu372Ala
ENST00000647938.1:c.3245A>C	ENSP00000498155.1:p.Glu1082Ala
ENST00000319584.10:c.1631A>C	ENSP00000313006.6:p.Glu544Ala
ENST00000346085.9:c.3245A>C	ENSP00000344546.4:p.Glu1082Ala
ENST00000350026.9:c.3206A>C	ENSP00000055163.7:p.Glu1069Ala
ENST00000400790.3:c.407A>C	ENSP00000383596.3:p.Glu136Ala
ENST00000414678.6:c.1772A>C	ENSP00000412835.2:p.Glu591Ala
ENST00000478761.3:c.816A>C
NM_017519.2:c.3206A>C	NP_059989.2:p.Glu1069Ala
NM_020732.3:c.3245A>C	NP_065783.3:p.Glu1082Ala
XM_005267069.3:c.3365A>C	XP_005267126.2:p.Glu1122Ala
XM_011535984.1:c.2444A>C	XP_011534286.1:p.Glu815Ala
XM_011535985.1:c.2264A>C	XP_011534287.1:p.Glu755Ala
XM_011535986.1:c.2024A>C	XP_011534288.1:p.Glu675Ala
XM_011535987.1:c.1643A>C	XP_011534289.1:p.Glu548Ala
XM_011535988.1:c.506A>C	XP_011534290.1:p.Glu169Ala
NM_001346813.1:c.3365A>C	NP_001333742.1:p.Glu1122Ala
NM_001363725.1:c.1115A>C	NP_001350654.1:p.Glu372Ala
XM_011535984.2:c.3575A>C	XP_011534286.2:p.Glu1192Ala
XM_011535988.3:c.506A>C	XP_011534290.1:p.Glu169Ala
XM_017011103.2:c.3476A>C	XP_016866592.1:p.Glu1159Ala
XM_017011104.1:c.3446A>C	XP_016866593.1:p.Glu1149Ala
XM_017011105.2:c.3416A>C	XP_016866594.1:p.Glu1139Ala
XM_017011106.2:c.3287A>C	XP_016866595.1:p.Glu1096Ala
XM_017011107.2:c.3266A>C	XP_016866596.1:p.Glu1089Ala
XR_002956289.1:n.3658A>C
NM_001363725.2:c.1115A>C	NP_001350654.1:p.Glu372Ala
NM_001371656.1:c.3494A>C	NP_001358585.1:p.Glu1165Ala
NM_001374820.1:c.3494A>C	NP_001361749.1:p.Glu1165Ala
NM_001374828.1:c.3614A>C MANE Select	NP_001361757.1:p.Glu1205Ala
NM_017519.3:c.3455A>C	NP_059989.3:p.Glu1152Ala