Canonical Allele Identifier: CA452781500

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510798C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189664C>A , CM000668.2:g.157189664C>A	GRCh38
NC_000006.11:g.157510798C>A , CM000668.1:g.157510798C>A	GRCh37
NC_000006.10:g.157552490C>A	NCBI36
NG_032093.1:g.416735C>A
NG_032093.2:g.416735C>A
NG_066624.1:g.418639C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3783C>A	ENSP00000055163.8:p.Gly1261=
ENST00000414678.8:c.3852C>A	ENSP00000412835.3:p.Gly1284=
ENST00000637015.2:c.4071C>A	ENSP00000489729.2:p.Gly1357=
ENST00000346085.10:c.3822C>A	ENSP00000344546.5:p.Gly1274=
ENST00000350026.10:c.3534C>A	ENSP00000055163.7:p.Gly1178=
ENST00000414678.7:c.2100C>A	ENSP00000412835.2:p.Gly700=
ENST00000635849.1:c.1263C>A	ENSP00000490948.1:p.Gly421=
ENST00000635957.1:c.897C>A	ENSP00000490385.1:p.Gly299=
ENST00000636930.2:c.3942C>A MANE Select	ENSP00000490491.2:p.Gly1314=
ENST00000636940.1:n.1939C>A
ENST00000637015.1:c.1310C>A
ENST00000637568.1:c.1224C>A
ENST00000637741.1:n.608C>A
ENST00000637810.1:c.1284C>A	ENSP00000489636.1:p.Gly428=
ENST00000637904.1:c.1443C>A	ENSP00000490550.1:p.Gly481=
ENST00000647938.1:c.3573C>A	ENSP00000498155.1:p.Gly1191=
ENST00000346085.9:c.3573C>A	ENSP00000344546.4:p.Gly1191=
ENST00000350026.9:c.3534C>A	ENSP00000055163.7:p.Gly1178=
ENST00000414678.6:c.2100C>A	ENSP00000412835.2:p.Gly700=
NM_017519.2:c.3534C>A	NP_059989.2:p.Gly1178=
NM_020732.3:c.3573C>A	NP_065783.3:p.Gly1191=
XM_005267069.3:c.3693C>A	XP_005267126.2:p.Gly1231=
XM_011535984.1:c.2772C>A	XP_011534286.1:p.Gly924=
XM_011535985.1:c.2592C>A	XP_011534287.1:p.Gly864=
XM_011535986.1:c.2352C>A	XP_011534288.1:p.Gly784=
XM_011535987.1:c.1971C>A	XP_011534289.1:p.Gly657=
XM_011535988.1:c.834C>A	XP_011534290.1:p.Gly278=
NM_001346813.1:c.3693C>A	NP_001333742.1:p.Gly1231=
NM_001363725.1:c.1443C>A	NP_001350654.1:p.Gly481=
XM_011535984.2:c.3903C>A	XP_011534286.2:p.Gly1301=
XM_011535988.3:c.834C>A	XP_011534290.1:p.Gly278=
XM_017011103.2:c.3804C>A	XP_016866592.1:p.Gly1268=
XM_017011104.1:c.3774C>A	XP_016866593.1:p.Gly1258=
XM_017011105.2:c.3744C>A	XP_016866594.1:p.Gly1248=
XM_017011106.2:c.3615C>A	XP_016866595.1:p.Gly1205=
XM_017011107.2:c.3594C>A	XP_016866596.1:p.Gly1198=
XR_002956289.1:n.3986C>A
NM_001363725.2:c.1443C>A	NP_001350654.1:p.Gly481=
NM_001371656.1:c.3822C>A	NP_001358585.1:p.Gly1274=
NM_001374820.1:c.3822C>A	NP_001361749.1:p.Gly1274=
NM_001374828.1:c.3942C>A MANE Select	NP_001361757.1:p.Gly1314=
NM_017519.3:c.3783C>A	NP_059989.3:p.Gly1261=