Canonical Allele Identifier: CA366241294

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235684
• COSMIC: COSM3859981 ; COSM3859982
• MyVariant Identifiers: chr6:g.157522085C>T (hg19) ; chr6:g.157200951C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200951C>T , CM000668.2:g.157200951C>T	GRCh38
NC_000006.11:g.157522085C>T , CM000668.1:g.157522085C>T	GRCh37
NC_000006.10:g.157563777C>T	NCBI36
NG_032093.1:g.428022C>T
NG_032093.2:g.428022C>T
NG_066624.1:g.429926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4567C>T	ENSP00000055163.8:p.Gln1523Ter
ENST00000414678.8:c.4636C>T	ENSP00000412835.3:p.Gln1546Ter
ENST00000637015.2:c.4855C>T	ENSP00000489729.2:p.Gln1619Ter
ENST00000346085.10:c.4606C>T	ENSP00000344546.5:p.Gln1536Ter
ENST00000350026.10:c.4318C>T	ENSP00000055163.7:p.Gln1440Ter
ENST00000414678.7:c.2884C>T	ENSP00000412835.2:p.Gln962Ter
ENST00000635849.1:c.2047C>T	ENSP00000490948.1:p.Gln683Ter
ENST00000635957.1:c.1678C>T	ENSP00000490385.1:p.Gln560Ter
ENST00000636227.1:n.3189C>T
ENST00000636254.1:n.646C>T
ENST00000636930.2:c.4726C>T MANE Select	ENSP00000490491.2:p.Gln1576Ter
ENST00000636940.1:n.2723C>T
ENST00000637015.1:c.2094C>T
ENST00000637568.1:c.2008C>T
ENST00000637741.1:n.1392C>T
ENST00000637810.1:c.2068C>T	ENSP00000489636.1:p.Gln690Ter
ENST00000637904.1:c.2227C>T	ENSP00000490550.1:p.Gln743Ter
ENST00000647938.1:c.4357C>T	ENSP00000498155.1:p.Gln1453Ter
ENST00000346085.9:c.4357C>T	ENSP00000344546.4:p.Gln1453Ter
ENST00000350026.9:c.4318C>T	ENSP00000055163.7:p.Gln1440Ter
ENST00000414678.6:c.2884C>T	ENSP00000412835.2:p.Gln962Ter
NM_017519.2:c.4318C>T	NP_059989.2:p.Gln1440Ter
NM_020732.3:c.4357C>T	NP_065783.3:p.Gln1453Ter
XM_005267069.3:c.4477C>T	XP_005267126.2:p.Gln1493Ter
XM_011535984.1:c.3556C>T	XP_011534286.1:p.Gln1186Ter
XM_011535985.1:c.3376C>T	XP_011534287.1:p.Gln1126Ter
XM_011535986.1:c.3136C>T	XP_011534288.1:p.Gln1046Ter
XM_011535987.1:c.2755C>T	XP_011534289.1:p.Gln919Ter
XM_011535988.1:c.1618C>T	XP_011534290.1:p.Gln540Ter
NM_001346813.1:c.4477C>T	NP_001333742.1:p.Gln1493Ter
NM_001363725.1:c.2227C>T	NP_001350654.1:p.Gln743Ter
XM_011535984.2:c.4687C>T	XP_011534286.2:p.Gln1563Ter
XM_011535988.3:c.1618C>T	XP_011534290.1:p.Gln540Ter
XM_017011103.2:c.4588C>T	XP_016866592.1:p.Gln1530Ter
XM_017011104.1:c.4558C>T	XP_016866593.1:p.Gln1520Ter
XM_017011105.2:c.4528C>T	XP_016866594.1:p.Gln1510Ter
XM_017011106.2:c.4399C>T	XP_016866595.1:p.Gln1467Ter
XM_017011107.2:c.4378C>T	XP_016866596.1:p.Gln1460Ter
XR_002956289.1:n.4673C>T
NM_001363725.2:c.2227C>T	NP_001350654.1:p.Gln743Ter
NM_001371656.1:c.4606C>T	NP_001358585.1:p.Gln1536Ter
NM_001374820.1:c.4606C>T	NP_001361749.1:p.Gln1536Ter
NM_001374828.1:c.4726C>T MANE Select	NP_001361757.1:p.Gln1576Ter
NM_017519.3:c.4567C>T	NP_059989.3:p.Gln1523Ter