Canonical Allele Identifier: CA366242136

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522293A>C (hg19) ; chr6:g.157201159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201159A>C , CM000668.2:g.157201159A>C	GRCh38
NC_000006.11:g.157522293A>C , CM000668.1:g.157522293A>C	GRCh37
NC_000006.10:g.157563985A>C	NCBI36
NG_032093.1:g.428230A>C
NG_032093.2:g.428230A>C
NG_066624.1:g.430134A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4775A>C	ENSP00000055163.8:p.Tyr1592Ser
ENST00000414678.8:c.4844A>C	ENSP00000412835.3:p.Tyr1615Ser
ENST00000637015.2:c.5063A>C	ENSP00000489729.2:p.Tyr1688Ser
ENST00000346085.10:c.4814A>C	ENSP00000344546.5:p.Tyr1605Ser
ENST00000350026.10:c.4526A>C	ENSP00000055163.7:p.Tyr1509Ser
ENST00000414678.7:c.3092A>C	ENSP00000412835.2:p.Tyr1031Ser
ENST00000635849.1:c.2255A>C	ENSP00000490948.1:p.Tyr752Ser
ENST00000635957.1:c.1886A>C	ENSP00000490385.1:p.Tyr629Ser
ENST00000636227.1:n.3397A>C
ENST00000636254.1:n.854A>C
ENST00000636930.2:c.4934A>C MANE Select	ENSP00000490491.2:p.Tyr1645Ser
ENST00000636940.1:n.2931A>C
ENST00000637015.1:c.2302A>C
ENST00000637568.1:c.2216A>C
ENST00000637741.1:n.1600A>C
ENST00000637810.1:c.2276A>C	ENSP00000489636.1:p.Tyr759Ser
ENST00000637904.1:c.2435A>C	ENSP00000490550.1:p.Tyr812Ser
ENST00000647938.1:c.4565A>C	ENSP00000498155.1:p.Tyr1522Ser
ENST00000346085.9:c.4565A>C	ENSP00000344546.4:p.Tyr1522Ser
ENST00000350026.9:c.4526A>C	ENSP00000055163.7:p.Tyr1509Ser
ENST00000414678.6:c.3092A>C	ENSP00000412835.2:p.Tyr1031Ser
NM_017519.2:c.4526A>C	NP_059989.2:p.Tyr1509Ser
NM_020732.3:c.4565A>C	NP_065783.3:p.Tyr1522Ser
XM_005267069.3:c.4685A>C	XP_005267126.2:p.Tyr1562Ser
XM_011535984.1:c.3764A>C	XP_011534286.1:p.Tyr1255Ser
XM_011535985.1:c.3584A>C	XP_011534287.1:p.Tyr1195Ser
XM_011535986.1:c.3344A>C	XP_011534288.1:p.Tyr1115Ser
XM_011535987.1:c.2963A>C	XP_011534289.1:p.Tyr988Ser
XM_011535988.1:c.1826A>C	XP_011534290.1:p.Tyr609Ser
NM_001346813.1:c.4685A>C	NP_001333742.1:p.Tyr1562Ser
NM_001363725.1:c.2435A>C	NP_001350654.1:p.Tyr812Ser
XM_011535984.2:c.4895A>C	XP_011534286.2:p.Tyr1632Ser
XM_011535988.3:c.1826A>C	XP_011534290.1:p.Tyr609Ser
XM_017011103.2:c.4796A>C	XP_016866592.1:p.Tyr1599Ser
XM_017011104.1:c.4766A>C	XP_016866593.1:p.Tyr1589Ser
XM_017011105.2:c.4736A>C	XP_016866594.1:p.Tyr1579Ser
XM_017011106.2:c.4607A>C	XP_016866595.1:p.Tyr1536Ser
XM_017011107.2:c.4586A>C	XP_016866596.1:p.Tyr1529Ser
XR_002956289.1:n.4881A>C
NM_001363725.2:c.2435A>C	NP_001350654.1:p.Tyr812Ser
NM_001371656.1:c.4814A>C	NP_001358585.1:p.Tyr1605Ser
NM_001374820.1:c.4814A>C	NP_001361749.1:p.Tyr1605Ser
NM_001374828.1:c.4934A>C MANE Select	NP_001361757.1:p.Tyr1645Ser
NM_017519.3:c.4775A>C	NP_059989.3:p.Tyr1592Ser