Canonical Allele Identifier: CA452978403

Gene: ARID1B

Linked Data

• dbSNP Id: rs759759957
• MyVariant Identifiers: chr6:g.157522189G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201055G>C , CM000668.2:g.157201055G>C	GRCh38
NC_000006.11:g.157522189G>C , CM000668.1:g.157522189G>C	GRCh37
NC_000006.10:g.157563881G>C	NCBI36
NG_032093.1:g.428126G>C
NG_032093.2:g.428126G>C
NG_066624.1:g.430030G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4671G>C	ENSP00000055163.8:p.Ala1557=
ENST00000414678.8:c.4740G>C	ENSP00000412835.3:p.Ala1580=
ENST00000637015.2:c.4959G>C	ENSP00000489729.2:p.Ala1653=
ENST00000346085.10:c.4710G>C	ENSP00000344546.5:p.Ala1570=
ENST00000350026.10:c.4422G>C	ENSP00000055163.7:p.Ala1474=
ENST00000414678.7:c.2988G>C	ENSP00000412835.2:p.Ala996=
ENST00000635849.1:c.2151G>C	ENSP00000490948.1:p.Ala717=
ENST00000635957.1:c.1782G>C	ENSP00000490385.1:p.Ala594=
ENST00000636227.1:n.3293G>C
ENST00000636254.1:n.750G>C
ENST00000636930.2:c.4830G>C MANE Select	ENSP00000490491.2:p.Ala1610=
ENST00000636940.1:n.2827G>C
ENST00000637015.1:c.2198G>C
ENST00000637568.1:c.2112G>C
ENST00000637741.1:n.1496G>C
ENST00000637810.1:c.2172G>C	ENSP00000489636.1:p.Ala724=
ENST00000637904.1:c.2331G>C	ENSP00000490550.1:p.Ala777=
ENST00000647938.1:c.4461G>C	ENSP00000498155.1:p.Ala1487=
ENST00000346085.9:c.4461G>C	ENSP00000344546.4:p.Ala1487=
ENST00000350026.9:c.4422G>C	ENSP00000055163.7:p.Ala1474=
ENST00000414678.6:c.2988G>C	ENSP00000412835.2:p.Ala996=
NM_017519.2:c.4422G>C	NP_059989.2:p.Ala1474=
NM_020732.3:c.4461G>C	NP_065783.3:p.Ala1487=
XM_005267069.3:c.4581G>C	XP_005267126.2:p.Ala1527=
XM_011535984.1:c.3660G>C	XP_011534286.1:p.Ala1220=
XM_011535985.1:c.3480G>C	XP_011534287.1:p.Ala1160=
XM_011535986.1:c.3240G>C	XP_011534288.1:p.Ala1080=
XM_011535987.1:c.2859G>C	XP_011534289.1:p.Ala953=
XM_011535988.1:c.1722G>C	XP_011534290.1:p.Ala574=
NM_001346813.1:c.4581G>C	NP_001333742.1:p.Ala1527=
NM_001363725.1:c.2331G>C	NP_001350654.1:p.Ala777=
XM_011535984.2:c.4791G>C	XP_011534286.2:p.Ala1597=
XM_011535988.3:c.1722G>C	XP_011534290.1:p.Ala574=
XM_017011103.2:c.4692G>C	XP_016866592.1:p.Ala1564=
XM_017011104.1:c.4662G>C	XP_016866593.1:p.Ala1554=
XM_017011105.2:c.4632G>C	XP_016866594.1:p.Ala1544=
XM_017011106.2:c.4503G>C	XP_016866595.1:p.Ala1501=
XM_017011107.2:c.4482G>C	XP_016866596.1:p.Ala1494=
XR_002956289.1:n.4777G>C
NM_001363725.2:c.2331G>C	NP_001350654.1:p.Ala777=
NM_001371656.1:c.4710G>C	NP_001358585.1:p.Ala1570=
NM_001374820.1:c.4710G>C	NP_001361749.1:p.Ala1570=
NM_001374828.1:c.4830G>C MANE Select	NP_001361757.1:p.Ala1610=
NM_017519.3:c.4671G>C	NP_059989.3:p.Ala1557=