Canonical Allele Identifier: CA366241765

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4678T>G	ENSP00000055163.8:p.Tyr1560Asp
ENST00000414678.8:c.4747T>G	ENSP00000412835.3:p.Tyr1583Asp
ENST00000637015.2:c.4966T>G	ENSP00000489729.2:p.Tyr1656Asp
ENST00000346085.10:c.4717T>G	ENSP00000344546.5:p.Tyr1573Asp
ENST00000350026.10:c.4429T>G	ENSP00000055163.7:p.Tyr1477Asp
ENST00000414678.7:c.2995T>G	ENSP00000412835.2:p.Tyr999Asp
ENST00000635849.1:c.2158T>G	ENSP00000490948.1:p.Tyr720Asp
ENST00000635957.1:c.1789T>G	ENSP00000490385.1:p.Tyr597Asp
ENST00000636227.1:n.3300T>G
ENST00000636254.1:n.757T>G
ENST00000636930.2:c.4837T>G MANE Select	ENSP00000490491.2:p.Tyr1613Asp
ENST00000636940.1:n.2834T>G
ENST00000637015.1:c.2205T>G
ENST00000637568.1:c.2119T>G
ENST00000637741.1:n.1503T>G
ENST00000637810.1:c.2179T>G	ENSP00000489636.1:p.Tyr727Asp
ENST00000637904.1:c.2338T>G	ENSP00000490550.1:p.Tyr780Asp
ENST00000647938.1:c.4468T>G	ENSP00000498155.1:p.Tyr1490Asp
ENST00000346085.9:c.4468T>G	ENSP00000344546.4:p.Tyr1490Asp
ENST00000350026.9:c.4429T>G	ENSP00000055163.7:p.Tyr1477Asp
ENST00000414678.6:c.2995T>G	ENSP00000412835.2:p.Tyr999Asp
NM_017519.2:c.4429T>G	NP_059989.2:p.Tyr1477Asp
NM_020732.3:c.4468T>G	NP_065783.3:p.Tyr1490Asp
XM_005267069.3:c.4588T>G	XP_005267126.2:p.Tyr1530Asp
XM_011535984.1:c.3667T>G	XP_011534286.1:p.Tyr1223Asp
XM_011535985.1:c.3487T>G	XP_011534287.1:p.Tyr1163Asp
XM_011535986.1:c.3247T>G	XP_011534288.1:p.Tyr1083Asp
XM_011535987.1:c.2866T>G	XP_011534289.1:p.Tyr956Asp
XM_011535988.1:c.1729T>G	XP_011534290.1:p.Tyr577Asp
NM_001346813.1:c.4588T>G	NP_001333742.1:p.Tyr1530Asp
NM_001363725.1:c.2338T>G	NP_001350654.1:p.Tyr780Asp
XM_011535984.2:c.4798T>G	XP_011534286.2:p.Tyr1600Asp
XM_011535988.3:c.1729T>G	XP_011534290.1:p.Tyr577Asp
XM_017011103.2:c.4699T>G	XP_016866592.1:p.Tyr1567Asp
XM_017011104.1:c.4669T>G	XP_016866593.1:p.Tyr1557Asp
XM_017011105.2:c.4639T>G	XP_016866594.1:p.Tyr1547Asp
XM_017011106.2:c.4510T>G	XP_016866595.1:p.Tyr1504Asp
XM_017011107.2:c.4489T>G	XP_016866596.1:p.Tyr1497Asp
XR_002956289.1:n.4784T>G
NM_001363725.2:c.2338T>G	NP_001350654.1:p.Tyr780Asp
NM_001371656.1:c.4717T>G	NP_001358585.1:p.Tyr1573Asp
NM_001374820.1:c.4717T>G	NP_001361749.1:p.Tyr1573Asp
NM_001374828.1:c.4837T>G MANE Select	NP_001361757.1:p.Tyr1613Asp
NM_017519.3:c.4678T>G	NP_059989.3:p.Tyr1560Asp