Canonical Allele Identifier: CA452978047

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794076476
• MyVariant Identifiers: chr6:g.157522237T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201103T>C , CM000668.2:g.157201103T>C	GRCh38
NC_000006.11:g.157522237T>C , CM000668.1:g.157522237T>C	GRCh37
NC_000006.10:g.157563929T>C	NCBI36
NG_032093.1:g.428174T>C
NG_032093.2:g.428174T>C
NG_066624.1:g.430078T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4719T>C	ENSP00000055163.8:p.Asp1573=
ENST00000414678.8:c.4788T>C	ENSP00000412835.3:p.Asp1596=
ENST00000637015.2:c.5007T>C	ENSP00000489729.2:p.Asp1669=
ENST00000346085.10:c.4758T>C	ENSP00000344546.5:p.Asp1586=
ENST00000350026.10:c.4470T>C	ENSP00000055163.7:p.Asp1490=
ENST00000414678.7:c.3036T>C	ENSP00000412835.2:p.Asp1012=
ENST00000635849.1:c.2199T>C	ENSP00000490948.1:p.Asp733=
ENST00000635957.1:c.1830T>C	ENSP00000490385.1:p.Asp610=
ENST00000636227.1:n.3341T>C
ENST00000636254.1:n.798T>C
ENST00000636930.2:c.4878T>C MANE Select	ENSP00000490491.2:p.Asp1626=
ENST00000636940.1:n.2875T>C
ENST00000637015.1:c.2246T>C
ENST00000637568.1:c.2160T>C
ENST00000637741.1:n.1544T>C
ENST00000637810.1:c.2220T>C	ENSP00000489636.1:p.Asp740=
ENST00000637904.1:c.2379T>C	ENSP00000490550.1:p.Asp793=
ENST00000647938.1:c.4509T>C	ENSP00000498155.1:p.Asp1503=
ENST00000346085.9:c.4509T>C	ENSP00000344546.4:p.Asp1503=
ENST00000350026.9:c.4470T>C	ENSP00000055163.7:p.Asp1490=
ENST00000414678.6:c.3036T>C	ENSP00000412835.2:p.Asp1012=
NM_017519.2:c.4470T>C	NP_059989.2:p.Asp1490=
NM_020732.3:c.4509T>C	NP_065783.3:p.Asp1503=
XM_005267069.3:c.4629T>C	XP_005267126.2:p.Asp1543=
XM_011535984.1:c.3708T>C	XP_011534286.1:p.Asp1236=
XM_011535985.1:c.3528T>C	XP_011534287.1:p.Asp1176=
XM_011535986.1:c.3288T>C	XP_011534288.1:p.Asp1096=
XM_011535987.1:c.2907T>C	XP_011534289.1:p.Asp969=
XM_011535988.1:c.1770T>C	XP_011534290.1:p.Asp590=
NM_001346813.1:c.4629T>C	NP_001333742.1:p.Asp1543=
NM_001363725.1:c.2379T>C	NP_001350654.1:p.Asp793=
XM_011535984.2:c.4839T>C	XP_011534286.2:p.Asp1613=
XM_011535988.3:c.1770T>C	XP_011534290.1:p.Asp590=
XM_017011103.2:c.4740T>C	XP_016866592.1:p.Asp1580=
XM_017011104.1:c.4710T>C	XP_016866593.1:p.Asp1570=
XM_017011105.2:c.4680T>C	XP_016866594.1:p.Asp1560=
XM_017011106.2:c.4551T>C	XP_016866595.1:p.Asp1517=
XM_017011107.2:c.4530T>C	XP_016866596.1:p.Asp1510=
XR_002956289.1:n.4825T>C
NM_001363725.2:c.2379T>C	NP_001350654.1:p.Asp793=
NM_001371656.1:c.4758T>C	NP_001358585.1:p.Asp1586=
NM_001374820.1:c.4758T>C	NP_001361749.1:p.Asp1586=
NM_001374828.1:c.4878T>C MANE Select	NP_001361757.1:p.Asp1626=
NM_017519.3:c.4719T>C	NP_059989.3:p.Asp1573=