Canonical Allele Identifier: CA150370248

Gene: ARID1B

Linked Data

• dbSNP Id: rs773006123
• MyVariant Identifiers: chr6:g.157522255G>C (hg19) ; chr6:g.157201121G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201121G>C , CM000668.2:g.157201121G>C	GRCh38
NC_000006.11:g.157522255G>C , CM000668.1:g.157522255G>C	GRCh37
NC_000006.10:g.157563947G>C	NCBI36
NG_032093.1:g.428192G>C
NG_032093.2:g.428192G>C
NG_066624.1:g.430096G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4737G>C	ENSP00000055163.8:p.Glu1579Asp
ENST00000414678.8:c.4806G>C	ENSP00000412835.3:p.Glu1602Asp
ENST00000637015.2:c.5025G>C	ENSP00000489729.2:p.Glu1675Asp
ENST00000346085.10:c.4776G>C	ENSP00000344546.5:p.Glu1592Asp
ENST00000350026.10:c.4488G>C	ENSP00000055163.7:p.Glu1496Asp
ENST00000414678.7:c.3054G>C	ENSP00000412835.2:p.Glu1018Asp
ENST00000635849.1:c.2217G>C	ENSP00000490948.1:p.Glu739Asp
ENST00000635957.1:c.1848G>C	ENSP00000490385.1:p.Glu616Asp
ENST00000636227.1:n.3359G>C
ENST00000636254.1:n.816G>C
ENST00000636930.2:c.4896G>C MANE Select	ENSP00000490491.2:p.Glu1632Asp
ENST00000636940.1:n.2893G>C
ENST00000637015.1:c.2264G>C
ENST00000637568.1:c.2178G>C
ENST00000637741.1:n.1562G>C
ENST00000637810.1:c.2238G>C	ENSP00000489636.1:p.Glu746Asp
ENST00000637904.1:c.2397G>C	ENSP00000490550.1:p.Glu799Asp
ENST00000647938.1:c.4527G>C	ENSP00000498155.1:p.Glu1509Asp
ENST00000346085.9:c.4527G>C	ENSP00000344546.4:p.Glu1509Asp
ENST00000350026.9:c.4488G>C	ENSP00000055163.7:p.Glu1496Asp
ENST00000414678.6:c.3054G>C	ENSP00000412835.2:p.Glu1018Asp
NM_017519.2:c.4488G>C	NP_059989.2:p.Glu1496Asp
NM_020732.3:c.4527G>C	NP_065783.3:p.Glu1509Asp
XM_005267069.3:c.4647G>C	XP_005267126.2:p.Glu1549Asp
XM_011535984.1:c.3726G>C	XP_011534286.1:p.Glu1242Asp
XM_011535985.1:c.3546G>C	XP_011534287.1:p.Glu1182Asp
XM_011535986.1:c.3306G>C	XP_011534288.1:p.Glu1102Asp
XM_011535987.1:c.2925G>C	XP_011534289.1:p.Glu975Asp
XM_011535988.1:c.1788G>C	XP_011534290.1:p.Glu596Asp
NM_001346813.1:c.4647G>C	NP_001333742.1:p.Glu1549Asp
NM_001363725.1:c.2397G>C	NP_001350654.1:p.Glu799Asp
XM_011535984.2:c.4857G>C	XP_011534286.2:p.Glu1619Asp
XM_011535988.3:c.1788G>C	XP_011534290.1:p.Glu596Asp
XM_017011103.2:c.4758G>C	XP_016866592.1:p.Glu1586Asp
XM_017011104.1:c.4728G>C	XP_016866593.1:p.Glu1576Asp
XM_017011105.2:c.4698G>C	XP_016866594.1:p.Glu1566Asp
XM_017011106.2:c.4569G>C	XP_016866595.1:p.Glu1523Asp
XM_017011107.2:c.4548G>C	XP_016866596.1:p.Glu1516Asp
XR_002956289.1:n.4843G>C
NM_001363725.2:c.2397G>C	NP_001350654.1:p.Glu799Asp
NM_001371656.1:c.4776G>C	NP_001358585.1:p.Glu1592Asp
NM_001374820.1:c.4776G>C	NP_001361749.1:p.Glu1592Asp
NM_001374828.1:c.4896G>C MANE Select	NP_001361757.1:p.Glu1632Asp
NM_017519.3:c.4737G>C	NP_059989.3:p.Glu1579Asp