Canonical Allele Identifier: CA366241769

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522196T>A (hg19) ; chr6:g.157201062T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201062T>A , CM000668.2:g.157201062T>A	GRCh38
NC_000006.11:g.157522196T>A , CM000668.1:g.157522196T>A	GRCh37
NC_000006.10:g.157563888T>A	NCBI36
NG_032093.1:g.428133T>A
NG_032093.2:g.428133T>A
NG_066624.1:g.430037T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4678T>A	ENSP00000055163.8:p.Tyr1560Asn
ENST00000414678.8:c.4747T>A	ENSP00000412835.3:p.Tyr1583Asn
ENST00000637015.2:c.4966T>A	ENSP00000489729.2:p.Tyr1656Asn
ENST00000346085.10:c.4717T>A	ENSP00000344546.5:p.Tyr1573Asn
ENST00000350026.10:c.4429T>A	ENSP00000055163.7:p.Tyr1477Asn
ENST00000414678.7:c.2995T>A	ENSP00000412835.2:p.Tyr999Asn
ENST00000635849.1:c.2158T>A	ENSP00000490948.1:p.Tyr720Asn
ENST00000635957.1:c.1789T>A	ENSP00000490385.1:p.Tyr597Asn
ENST00000636227.1:n.3300T>A
ENST00000636254.1:n.757T>A
ENST00000636930.2:c.4837T>A MANE Select	ENSP00000490491.2:p.Tyr1613Asn
ENST00000636940.1:n.2834T>A
ENST00000637015.1:c.2205T>A
ENST00000637568.1:c.2119T>A
ENST00000637741.1:n.1503T>A
ENST00000637810.1:c.2179T>A	ENSP00000489636.1:p.Tyr727Asn
ENST00000637904.1:c.2338T>A	ENSP00000490550.1:p.Tyr780Asn
ENST00000647938.1:c.4468T>A	ENSP00000498155.1:p.Tyr1490Asn
ENST00000346085.9:c.4468T>A	ENSP00000344546.4:p.Tyr1490Asn
ENST00000350026.9:c.4429T>A	ENSP00000055163.7:p.Tyr1477Asn
ENST00000414678.6:c.2995T>A	ENSP00000412835.2:p.Tyr999Asn
NM_017519.2:c.4429T>A	NP_059989.2:p.Tyr1477Asn
NM_020732.3:c.4468T>A	NP_065783.3:p.Tyr1490Asn
XM_005267069.3:c.4588T>A	XP_005267126.2:p.Tyr1530Asn
XM_011535984.1:c.3667T>A	XP_011534286.1:p.Tyr1223Asn
XM_011535985.1:c.3487T>A	XP_011534287.1:p.Tyr1163Asn
XM_011535986.1:c.3247T>A	XP_011534288.1:p.Tyr1083Asn
XM_011535987.1:c.2866T>A	XP_011534289.1:p.Tyr956Asn
XM_011535988.1:c.1729T>A	XP_011534290.1:p.Tyr577Asn
NM_001346813.1:c.4588T>A	NP_001333742.1:p.Tyr1530Asn
NM_001363725.1:c.2338T>A	NP_001350654.1:p.Tyr780Asn
XM_011535984.2:c.4798T>A	XP_011534286.2:p.Tyr1600Asn
XM_011535988.3:c.1729T>A	XP_011534290.1:p.Tyr577Asn
XM_017011103.2:c.4699T>A	XP_016866592.1:p.Tyr1567Asn
XM_017011104.1:c.4669T>A	XP_016866593.1:p.Tyr1557Asn
XM_017011105.2:c.4639T>A	XP_016866594.1:p.Tyr1547Asn
XM_017011106.2:c.4510T>A	XP_016866595.1:p.Tyr1504Asn
XM_017011107.2:c.4489T>A	XP_016866596.1:p.Tyr1497Asn
XR_002956289.1:n.4784T>A
NM_001363725.2:c.2338T>A	NP_001350654.1:p.Tyr780Asn
NM_001371656.1:c.4717T>A	NP_001358585.1:p.Tyr1573Asn
NM_001374820.1:c.4717T>A	NP_001361749.1:p.Tyr1573Asn
NM_001374828.1:c.4837T>A MANE Select	NP_001361757.1:p.Tyr1613Asn
NM_017519.3:c.4678T>A	NP_059989.3:p.Tyr1560Asn