Canonical Allele Identifier: CA452978036

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157505442G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184308G>T , CM000668.2:g.157184308G>T	GRCh38
NC_000006.11:g.157505442G>T , CM000668.1:g.157505442G>T	GRCh37
NC_000006.10:g.157547134G>T	NCBI36
NG_032093.1:g.411379G>T
NG_032093.2:g.411379G>T
NG_066624.1:g.413283G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3633G>T	ENSP00000055163.8:p.Leu1211=
ENST00000414678.8:c.3702G>T	ENSP00000412835.3:p.Leu1234=
ENST00000637015.2:c.3921G>T	ENSP00000489729.2:p.Leu1307=
ENST00000319584.11:c.1806G>T	ENSP00000313006.7:p.Leu602=
ENST00000346085.10:c.3672G>T	ENSP00000344546.5:p.Leu1224=
ENST00000350026.10:c.3384G>T	ENSP00000055163.7:p.Leu1128=
ENST00000414678.7:c.1950G>T	ENSP00000412835.2:p.Leu650=
ENST00000635849.1:c.1113G>T	ENSP00000490948.1:p.Leu371=
ENST00000635957.1:c.747G>T	ENSP00000490385.1:p.Leu249=
ENST00000636930.2:c.3792G>T MANE Select	ENSP00000490491.2:p.Leu1264=
ENST00000636940.1:n.1789G>T
ENST00000637015.1:c.1160G>T
ENST00000637568.1:c.1074G>T
ENST00000637741.1:n.458G>T
ENST00000637810.1:c.1134G>T	ENSP00000489636.1:p.Leu378=
ENST00000637904.1:c.1293G>T	ENSP00000490550.1:p.Leu431=
ENST00000647938.1:c.3423G>T	ENSP00000498155.1:p.Leu1141=
ENST00000319584.10:c.1809G>T	ENSP00000313006.6:p.Leu603=
ENST00000346085.9:c.3423G>T	ENSP00000344546.4:p.Leu1141=
ENST00000350026.9:c.3384G>T	ENSP00000055163.7:p.Leu1128=
ENST00000400790.3:c.585G>T	ENSP00000383596.3:p.Leu195=
ENST00000414678.6:c.1950G>T	ENSP00000412835.2:p.Leu650=
NM_017519.2:c.3384G>T	NP_059989.2:p.Leu1128=
NM_020732.3:c.3423G>T	NP_065783.3:p.Leu1141=
XM_005267069.3:c.3543G>T	XP_005267126.2:p.Leu1181=
XM_011535984.1:c.2622G>T	XP_011534286.1:p.Leu874=
XM_011535985.1:c.2442G>T	XP_011534287.1:p.Leu814=
XM_011535986.1:c.2202G>T	XP_011534288.1:p.Leu734=
XM_011535987.1:c.1821G>T	XP_011534289.1:p.Leu607=
XM_011535988.1:c.684G>T	XP_011534290.1:p.Leu228=
NM_001346813.1:c.3543G>T	NP_001333742.1:p.Leu1181=
NM_001363725.1:c.1293G>T	NP_001350654.1:p.Leu431=
XM_011535984.2:c.3753G>T	XP_011534286.2:p.Leu1251=
XM_011535988.3:c.684G>T	XP_011534290.1:p.Leu228=
XM_017011103.2:c.3654G>T	XP_016866592.1:p.Leu1218=
XM_017011104.1:c.3624G>T	XP_016866593.1:p.Leu1208=
XM_017011105.2:c.3594G>T	XP_016866594.1:p.Leu1198=
XM_017011106.2:c.3465G>T	XP_016866595.1:p.Leu1155=
XM_017011107.2:c.3444G>T	XP_016866596.1:p.Leu1148=
XR_002956289.1:n.3836G>T
NM_001363725.2:c.1293G>T	NP_001350654.1:p.Leu431=
NM_001371656.1:c.3672G>T	NP_001358585.1:p.Leu1224=
NM_001374820.1:c.3672G>T	NP_001361749.1:p.Leu1224=
NM_001374828.1:c.3792G>T MANE Select	NP_001361757.1:p.Leu1264=
NM_017519.3:c.3633G>T	NP_059989.3:p.Leu1211=