Canonical Allele Identifier: CA366241127

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522010A>C (hg19) ; chr6:g.157200876A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200876A>C , CM000668.2:g.157200876A>C	GRCh38
NC_000006.11:g.157522010A>C , CM000668.1:g.157522010A>C	GRCh37
NC_000006.10:g.157563702A>C	NCBI36
NG_032093.1:g.427947A>C
NG_032093.2:g.427947A>C
NG_066624.1:g.429851A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4492A>C	ENSP00000055163.8:p.Ser1498Arg
ENST00000414678.8:c.4561A>C	ENSP00000412835.3:p.Ser1521Arg
ENST00000637015.2:c.4780A>C	ENSP00000489729.2:p.Ser1594Arg
ENST00000346085.10:c.4531A>C	ENSP00000344546.5:p.Ser1511Arg
ENST00000350026.10:c.4243A>C	ENSP00000055163.7:p.Ser1415Arg
ENST00000414678.7:c.2809A>C	ENSP00000412835.2:p.Ser937Arg
ENST00000635849.1:c.1972A>C	ENSP00000490948.1:p.Ser658Arg
ENST00000635957.1:c.1603A>C	ENSP00000490385.1:p.Ser535Arg
ENST00000636227.1:n.3114A>C
ENST00000636254.1:n.571A>C
ENST00000636930.2:c.4651A>C MANE Select	ENSP00000490491.2:p.Ser1551Arg
ENST00000636940.1:n.2648A>C
ENST00000637015.1:c.2019A>C
ENST00000637568.1:c.1933A>C
ENST00000637741.1:n.1317A>C
ENST00000637810.1:c.1993A>C	ENSP00000489636.1:p.Ser665Arg
ENST00000637904.1:c.2152A>C	ENSP00000490550.1:p.Ser718Arg
ENST00000647938.1:c.4282A>C	ENSP00000498155.1:p.Ser1428Arg
ENST00000346085.9:c.4282A>C	ENSP00000344546.4:p.Ser1428Arg
ENST00000350026.9:c.4243A>C	ENSP00000055163.7:p.Ser1415Arg
ENST00000414678.6:c.2809A>C	ENSP00000412835.2:p.Ser937Arg
NM_017519.2:c.4243A>C	NP_059989.2:p.Ser1415Arg
NM_020732.3:c.4282A>C	NP_065783.3:p.Ser1428Arg
XM_005267069.3:c.4402A>C	XP_005267126.2:p.Ser1468Arg
XM_011535984.1:c.3481A>C	XP_011534286.1:p.Ser1161Arg
XM_011535985.1:c.3301A>C	XP_011534287.1:p.Ser1101Arg
XM_011535986.1:c.3061A>C	XP_011534288.1:p.Ser1021Arg
XM_011535987.1:c.2680A>C	XP_011534289.1:p.Ser894Arg
XM_011535988.1:c.1543A>C	XP_011534290.1:p.Ser515Arg
NM_001346813.1:c.4402A>C	NP_001333742.1:p.Ser1468Arg
NM_001363725.1:c.2152A>C	NP_001350654.1:p.Ser718Arg
XM_011535984.2:c.4612A>C	XP_011534286.2:p.Ser1538Arg
XM_011535988.3:c.1543A>C	XP_011534290.1:p.Ser515Arg
XM_017011103.2:c.4513A>C	XP_016866592.1:p.Ser1505Arg
XM_017011104.1:c.4483A>C	XP_016866593.1:p.Ser1495Arg
XM_017011105.2:c.4453A>C	XP_016866594.1:p.Ser1485Arg
XM_017011106.2:c.4324A>C	XP_016866595.1:p.Ser1442Arg
XM_017011107.2:c.4303A>C	XP_016866596.1:p.Ser1435Arg
XR_002956289.1:n.4598A>C
NM_001363725.2:c.2152A>C	NP_001350654.1:p.Ser718Arg
NM_001371656.1:c.4531A>C	NP_001358585.1:p.Ser1511Arg
NM_001374820.1:c.4531A>C	NP_001361749.1:p.Ser1511Arg
NM_001374828.1:c.4651A>C MANE Select	NP_001361757.1:p.Ser1551Arg
NM_017519.3:c.4492A>C	NP_059989.3:p.Ser1498Arg