Canonical Allele Identifier: CA366227331

Gene: ARID1B

Linked Data

• COSMIC: COSM6380017 ; COSM6380018
• MyVariant Identifiers: chr6:g.157502155T>C (hg19) ; chr6:g.157181021T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181021T>C , CM000668.2:g.157181021T>C	GRCh38
NC_000006.11:g.157502155T>C , CM000668.1:g.157502155T>C	GRCh37
NC_000006.10:g.157543847T>C	NCBI36
NG_032093.1:g.408092T>C
NG_032093.2:g.408092T>C
NG_066624.1:g.409996T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3398T>C	ENSP00000055163.8:p.Leu1133Pro
ENST00000414678.8:c.3467T>C	ENSP00000412835.3:p.Leu1156Pro
ENST00000637015.2:c.3686T>C	ENSP00000489729.2:p.Leu1229Pro
ENST00000319584.11:c.1571T>C	ENSP00000313006.7:p.Leu524Pro
ENST00000346085.10:c.3437T>C	ENSP00000344546.5:p.Leu1146Pro
ENST00000350026.10:c.3149T>C	ENSP00000055163.7:p.Leu1050Pro
ENST00000414678.7:c.1715T>C	ENSP00000412835.2:p.Leu572Pro
ENST00000635849.1:c.878T>C	ENSP00000490948.1:p.Leu293Pro
ENST00000635957.1:c.512T>C	ENSP00000490385.1:p.Leu171Pro
ENST00000636930.2:c.3557T>C MANE Select	ENSP00000490491.2:p.Leu1186Pro
ENST00000636940.1:n.1554T>C
ENST00000637015.1:c.925T>C
ENST00000637568.1:c.839T>C
ENST00000637741.1:n.223T>C
ENST00000637810.1:c.899T>C	ENSP00000489636.1:p.Leu300Pro
ENST00000637904.1:c.1058T>C	ENSP00000490550.1:p.Leu353Pro
ENST00000647938.1:c.3188T>C	ENSP00000498155.1:p.Leu1063Pro
ENST00000319584.10:c.1574T>C	ENSP00000313006.6:p.Leu525Pro
ENST00000346085.9:c.3188T>C	ENSP00000344546.4:p.Leu1063Pro
ENST00000350026.9:c.3149T>C	ENSP00000055163.7:p.Leu1050Pro
ENST00000400790.3:c.350T>C	ENSP00000383596.3:p.Leu117Pro
ENST00000414678.6:c.1715T>C	ENSP00000412835.2:p.Leu572Pro
ENST00000478761.3:c.759T>C
NM_017519.2:c.3149T>C	NP_059989.2:p.Leu1050Pro
NM_020732.3:c.3188T>C	NP_065783.3:p.Leu1063Pro
XM_005267069.3:c.3308T>C	XP_005267126.2:p.Leu1103Pro
XM_011535984.1:c.2387T>C	XP_011534286.1:p.Leu796Pro
XM_011535985.1:c.2207T>C	XP_011534287.1:p.Leu736Pro
XM_011535986.1:c.1967T>C	XP_011534288.1:p.Leu656Pro
XM_011535987.1:c.1586T>C	XP_011534289.1:p.Leu529Pro
XM_011535988.1:c.449T>C	XP_011534290.1:p.Leu150Pro
NM_001346813.1:c.3308T>C	NP_001333742.1:p.Leu1103Pro
NM_001363725.1:c.1058T>C	NP_001350654.1:p.Leu353Pro
XM_011535984.2:c.3518T>C	XP_011534286.2:p.Leu1173Pro
XM_011535988.3:c.449T>C	XP_011534290.1:p.Leu150Pro
XM_017011103.2:c.3419T>C	XP_016866592.1:p.Leu1140Pro
XM_017011104.1:c.3389T>C	XP_016866593.1:p.Leu1130Pro
XM_017011105.2:c.3359T>C	XP_016866594.1:p.Leu1120Pro
XM_017011106.2:c.3230T>C	XP_016866595.1:p.Leu1077Pro
XM_017011107.2:c.3209T>C	XP_016866596.1:p.Leu1070Pro
XR_002956289.1:n.3601T>C
NM_001363725.2:c.1058T>C	NP_001350654.1:p.Leu353Pro
NM_001371656.1:c.3437T>C	NP_001358585.1:p.Leu1146Pro
NM_001374820.1:c.3437T>C	NP_001361749.1:p.Leu1146Pro
NM_001374828.1:c.3557T>C MANE Select	NP_001361757.1:p.Leu1186Pro
NM_017519.3:c.3398T>C	NP_059989.3:p.Leu1133Pro