Canonical Allele Identifier: CA452781487

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510777T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189643T>G , CM000668.2:g.157189643T>G	GRCh38
NC_000006.11:g.157510777T>G , CM000668.1:g.157510777T>G	GRCh37
NC_000006.10:g.157552469T>G	NCBI36
NG_032093.1:g.416714T>G
NG_032093.2:g.416714T>G
NG_066624.1:g.418618T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3762T>G	ENSP00000055163.8:p.Ala1254=
ENST00000414678.8:c.3831T>G	ENSP00000412835.3:p.Ala1277=
ENST00000637015.2:c.4050T>G	ENSP00000489729.2:p.Ala1350=
ENST00000346085.10:c.3801T>G	ENSP00000344546.5:p.Ala1267=
ENST00000350026.10:c.3513T>G	ENSP00000055163.7:p.Ala1171=
ENST00000414678.7:c.2079T>G	ENSP00000412835.2:p.Ala693=
ENST00000635849.1:c.1242T>G	ENSP00000490948.1:p.Ala414=
ENST00000635957.1:c.876T>G	ENSP00000490385.1:p.Ala292=
ENST00000636930.2:c.3921T>G MANE Select	ENSP00000490491.2:p.Ala1307=
ENST00000636940.1:n.1918T>G
ENST00000637015.1:c.1289T>G
ENST00000637568.1:c.1203T>G
ENST00000637741.1:n.587T>G
ENST00000637810.1:c.1263T>G	ENSP00000489636.1:p.Ala421=
ENST00000637904.1:c.1422T>G	ENSP00000490550.1:p.Ala474=
ENST00000647938.1:c.3552T>G	ENSP00000498155.1:p.Ala1184=
ENST00000346085.9:c.3552T>G	ENSP00000344546.4:p.Ala1184=
ENST00000350026.9:c.3513T>G	ENSP00000055163.7:p.Ala1171=
ENST00000414678.6:c.2079T>G	ENSP00000412835.2:p.Ala693=
NM_017519.2:c.3513T>G	NP_059989.2:p.Ala1171=
NM_020732.3:c.3552T>G	NP_065783.3:p.Ala1184=
XM_005267069.3:c.3672T>G	XP_005267126.2:p.Ala1224=
XM_011535984.1:c.2751T>G	XP_011534286.1:p.Ala917=
XM_011535985.1:c.2571T>G	XP_011534287.1:p.Ala857=
XM_011535986.1:c.2331T>G	XP_011534288.1:p.Ala777=
XM_011535987.1:c.1950T>G	XP_011534289.1:p.Ala650=
XM_011535988.1:c.813T>G	XP_011534290.1:p.Ala271=
NM_001346813.1:c.3672T>G	NP_001333742.1:p.Ala1224=
NM_001363725.1:c.1422T>G	NP_001350654.1:p.Ala474=
XM_011535984.2:c.3882T>G	XP_011534286.2:p.Ala1294=
XM_011535988.3:c.813T>G	XP_011534290.1:p.Ala271=
XM_017011103.2:c.3783T>G	XP_016866592.1:p.Ala1261=
XM_017011104.1:c.3753T>G	XP_016866593.1:p.Ala1251=
XM_017011105.2:c.3723T>G	XP_016866594.1:p.Ala1241=
XM_017011106.2:c.3594T>G	XP_016866595.1:p.Ala1198=
XM_017011107.2:c.3573T>G	XP_016866596.1:p.Ala1191=
XR_002956289.1:n.3965T>G
NM_001363725.2:c.1422T>G	NP_001350654.1:p.Ala474=
NM_001371656.1:c.3801T>G	NP_001358585.1:p.Ala1267=
NM_001374820.1:c.3801T>G	NP_001361749.1:p.Ala1267=
NM_001374828.1:c.3921T>G MANE Select	NP_001361757.1:p.Ala1307=
NM_017519.3:c.3762T>G	NP_059989.3:p.Ala1254=