Canonical Allele Identifier: CA366239776

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157520004A>C (hg19) ; chr6:g.157198870A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198870A>C , CM000668.2:g.157198870A>C	GRCh38
NC_000006.11:g.157520004A>C , CM000668.1:g.157520004A>C	GRCh37
NC_000006.10:g.157561696A>C	NCBI36
NG_032093.1:g.425941A>C
NG_032093.2:g.425941A>C
NG_066624.1:g.427845A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4283A>C	ENSP00000055163.8:p.Tyr1428Ser
ENST00000414678.8:c.4352A>C	ENSP00000412835.3:p.Tyr1451Ser
ENST00000637015.2:c.4571A>C	ENSP00000489729.2:p.Tyr1524Ser
ENST00000346085.10:c.4322A>C	ENSP00000344546.5:p.Tyr1441Ser
ENST00000350026.10:c.4034A>C	ENSP00000055163.7:p.Tyr1345Ser
ENST00000414678.7:c.2600A>C	ENSP00000412835.2:p.Tyr867Ser
ENST00000635849.1:c.1763A>C	ENSP00000490948.1:p.Tyr588Ser
ENST00000635957.1:c.1394A>C	ENSP00000490385.1:p.Tyr465Ser
ENST00000636227.1:n.2905A>C
ENST00000636254.1:n.362A>C
ENST00000636930.2:c.4442A>C MANE Select	ENSP00000490491.2:p.Tyr1481Ser
ENST00000636940.1:n.2439A>C
ENST00000637015.1:c.1810A>C
ENST00000637568.1:c.1724A>C
ENST00000637741.1:n.1108A>C
ENST00000637810.1:c.1784A>C	ENSP00000489636.1:p.Tyr595Ser
ENST00000637904.1:c.1943A>C	ENSP00000490550.1:p.Tyr648Ser
ENST00000647938.1:c.4073A>C	ENSP00000498155.1:p.Tyr1358Ser
ENST00000346085.9:c.4073A>C	ENSP00000344546.4:p.Tyr1358Ser
ENST00000350026.9:c.4034A>C	ENSP00000055163.7:p.Tyr1345Ser
ENST00000414678.6:c.2600A>C	ENSP00000412835.2:p.Tyr867Ser
NM_017519.2:c.4034A>C	NP_059989.2:p.Tyr1345Ser
NM_020732.3:c.4073A>C	NP_065783.3:p.Tyr1358Ser
XM_005267069.3:c.4193A>C	XP_005267126.2:p.Tyr1398Ser
XM_011535984.1:c.3272A>C	XP_011534286.1:p.Tyr1091Ser
XM_011535985.1:c.3092A>C	XP_011534287.1:p.Tyr1031Ser
XM_011535986.1:c.2852A>C	XP_011534288.1:p.Tyr951Ser
XM_011535987.1:c.2471A>C	XP_011534289.1:p.Tyr824Ser
XM_011535988.1:c.1334A>C	XP_011534290.1:p.Tyr445Ser
NM_001346813.1:c.4193A>C	NP_001333742.1:p.Tyr1398Ser
NM_001363725.1:c.1943A>C	NP_001350654.1:p.Tyr648Ser
XM_011535984.2:c.4403A>C	XP_011534286.2:p.Tyr1468Ser
XM_011535988.3:c.1334A>C	XP_011534290.1:p.Tyr445Ser
XM_017011103.2:c.4304A>C	XP_016866592.1:p.Tyr1435Ser
XM_017011104.1:c.4274A>C	XP_016866593.1:p.Tyr1425Ser
XM_017011105.2:c.4244A>C	XP_016866594.1:p.Tyr1415Ser
XM_017011106.2:c.4115A>C	XP_016866595.1:p.Tyr1372Ser
XM_017011107.2:c.4094A>C	XP_016866596.1:p.Tyr1365Ser
XR_002956289.1:n.4427-1835A>C
NM_001363725.2:c.1943A>C	NP_001350654.1:p.Tyr648Ser
NM_001371656.1:c.4322A>C	NP_001358585.1:p.Tyr1441Ser
NM_001374820.1:c.4322A>C	NP_001361749.1:p.Tyr1441Ser
NM_001374828.1:c.4442A>C MANE Select	NP_001361757.1:p.Tyr1481Ser
NM_017519.3:c.4283A>C	NP_059989.3:p.Tyr1428Ser