Canonical Allele Identifier: CA452780745

Gene: ARID1B

Linked Data

• dbSNP Id: rs747533804
• MyVariant Identifiers: chr6:g.157502156G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181022G>T , CM000668.2:g.157181022G>T	GRCh38
NC_000006.11:g.157502156G>T , CM000668.1:g.157502156G>T	GRCh37
NC_000006.10:g.157543848G>T	NCBI36
NG_032093.1:g.408093G>T
NG_032093.2:g.408093G>T
NG_066624.1:g.409997G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3399G>T	ENSP00000055163.8:p.Leu1133=
ENST00000414678.8:c.3468G>T	ENSP00000412835.3:p.Leu1156=
ENST00000637015.2:c.3687G>T	ENSP00000489729.2:p.Leu1229=
ENST00000319584.11:c.1572G>T	ENSP00000313006.7:p.Leu524=
ENST00000346085.10:c.3438G>T	ENSP00000344546.5:p.Leu1146=
ENST00000350026.10:c.3150G>T	ENSP00000055163.7:p.Leu1050=
ENST00000414678.7:c.1716G>T	ENSP00000412835.2:p.Leu572=
ENST00000635849.1:c.879G>T	ENSP00000490948.1:p.Leu293=
ENST00000635957.1:c.513G>T	ENSP00000490385.1:p.Leu171=
ENST00000636930.2:c.3558G>T MANE Select	ENSP00000490491.2:p.Leu1186=
ENST00000636940.1:n.1555G>T
ENST00000637015.1:c.926G>T
ENST00000637568.1:c.840G>T
ENST00000637741.1:n.224G>T
ENST00000637810.1:c.900G>T	ENSP00000489636.1:p.Leu300=
ENST00000637904.1:c.1059G>T	ENSP00000490550.1:p.Leu353=
ENST00000647938.1:c.3189G>T	ENSP00000498155.1:p.Leu1063=
ENST00000319584.10:c.1575G>T	ENSP00000313006.6:p.Leu525=
ENST00000346085.9:c.3189G>T	ENSP00000344546.4:p.Leu1063=
ENST00000350026.9:c.3150G>T	ENSP00000055163.7:p.Leu1050=
ENST00000400790.3:c.351G>T	ENSP00000383596.3:p.Leu117=
ENST00000414678.6:c.1716G>T	ENSP00000412835.2:p.Leu572=
ENST00000478761.3:c.760G>T
NM_017519.2:c.3150G>T	NP_059989.2:p.Leu1050=
NM_020732.3:c.3189G>T	NP_065783.3:p.Leu1063=
XM_005267069.3:c.3309G>T	XP_005267126.2:p.Leu1103=
XM_011535984.1:c.2388G>T	XP_011534286.1:p.Leu796=
XM_011535985.1:c.2208G>T	XP_011534287.1:p.Leu736=
XM_011535986.1:c.1968G>T	XP_011534288.1:p.Leu656=
XM_011535987.1:c.1587G>T	XP_011534289.1:p.Leu529=
XM_011535988.1:c.450G>T	XP_011534290.1:p.Leu150=
NM_001346813.1:c.3309G>T	NP_001333742.1:p.Leu1103=
NM_001363725.1:c.1059G>T	NP_001350654.1:p.Leu353=
XM_011535984.2:c.3519G>T	XP_011534286.2:p.Leu1173=
XM_011535988.3:c.450G>T	XP_011534290.1:p.Leu150=
XM_017011103.2:c.3420G>T	XP_016866592.1:p.Leu1140=
XM_017011104.1:c.3390G>T	XP_016866593.1:p.Leu1130=
XM_017011105.2:c.3360G>T	XP_016866594.1:p.Leu1120=
XM_017011106.2:c.3231G>T	XP_016866595.1:p.Leu1077=
XM_017011107.2:c.3210G>T	XP_016866596.1:p.Leu1070=
XR_002956289.1:n.3602G>T
NM_001363725.2:c.1059G>T	NP_001350654.1:p.Leu353=
NM_001371656.1:c.3438G>T	NP_001358585.1:p.Leu1146=
NM_001374820.1:c.3438G>T	NP_001361749.1:p.Leu1146=
NM_001374828.1:c.3558G>T MANE Select	NP_001361757.1:p.Leu1186=
NM_017519.3:c.3399G>T	NP_059989.3:p.Leu1133=