Canonical Allele Identifier: CA452781553

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510873C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189739C>A , CM000668.2:g.157189739C>A	GRCh38
NC_000006.11:g.157510873C>A , CM000668.1:g.157510873C>A	GRCh37
NC_000006.10:g.157552565C>A	NCBI36
NG_032093.1:g.416810C>A
NG_032093.2:g.416810C>A
NG_066624.1:g.418714C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3858C>A	ENSP00000055163.8:p.Ala1286=
ENST00000414678.8:c.3927C>A	ENSP00000412835.3:p.Ala1309=
ENST00000637015.2:c.4146C>A	ENSP00000489729.2:p.Ala1382=
ENST00000346085.10:c.3897C>A	ENSP00000344546.5:p.Ala1299=
ENST00000350026.10:c.3609C>A	ENSP00000055163.7:p.Ala1203=
ENST00000414678.7:c.2175C>A	ENSP00000412835.2:p.Ala725=
ENST00000635849.1:c.1338C>A	ENSP00000490948.1:p.Ala446=
ENST00000635957.1:c.972C>A	ENSP00000490385.1:p.Ala324=
ENST00000636930.2:c.4017C>A MANE Select	ENSP00000490491.2:p.Ala1339=
ENST00000636940.1:n.2014C>A
ENST00000637015.1:c.1385C>A
ENST00000637568.1:c.1299C>A
ENST00000637741.1:n.683C>A
ENST00000637810.1:c.1359C>A	ENSP00000489636.1:p.Ala453=
ENST00000637904.1:c.1518C>A	ENSP00000490550.1:p.Ala506=
ENST00000647938.1:c.3648C>A	ENSP00000498155.1:p.Ala1216=
ENST00000346085.9:c.3648C>A	ENSP00000344546.4:p.Ala1216=
ENST00000350026.9:c.3609C>A	ENSP00000055163.7:p.Ala1203=
ENST00000414678.6:c.2175C>A	ENSP00000412835.2:p.Ala725=
NM_017519.2:c.3609C>A	NP_059989.2:p.Ala1203=
NM_020732.3:c.3648C>A	NP_065783.3:p.Ala1216=
XM_005267069.3:c.3768C>A	XP_005267126.2:p.Ala1256=
XM_011535984.1:c.2847C>A	XP_011534286.1:p.Ala949=
XM_011535985.1:c.2667C>A	XP_011534287.1:p.Ala889=
XM_011535986.1:c.2427C>A	XP_011534288.1:p.Ala809=
XM_011535987.1:c.2046C>A	XP_011534289.1:p.Ala682=
XM_011535988.1:c.909C>A	XP_011534290.1:p.Ala303=
NM_001346813.1:c.3768C>A	NP_001333742.1:p.Ala1256=
NM_001363725.1:c.1518C>A	NP_001350654.1:p.Ala506=
XM_011535984.2:c.3978C>A	XP_011534286.2:p.Ala1326=
XM_011535988.3:c.909C>A	XP_011534290.1:p.Ala303=
XM_017011103.2:c.3879C>A	XP_016866592.1:p.Ala1293=
XM_017011104.1:c.3849C>A	XP_016866593.1:p.Ala1283=
XM_017011105.2:c.3819C>A	XP_016866594.1:p.Ala1273=
XM_017011106.2:c.3690C>A	XP_016866595.1:p.Ala1230=
XM_017011107.2:c.3669C>A	XP_016866596.1:p.Ala1223=
XR_002956289.1:n.4061C>A
NM_001363725.2:c.1518C>A	NP_001350654.1:p.Ala506=
NM_001371656.1:c.3897C>A	NP_001358585.1:p.Ala1299=
NM_001374820.1:c.3897C>A	NP_001361749.1:p.Ala1299=
NM_001374828.1:c.4017C>A MANE Select	NP_001361757.1:p.Ala1339=
NM_017519.3:c.3858C>A	NP_059989.3:p.Ala1286=