Canonical Allele Identifier: CA452783926

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366092
• MyVariant Identifiers: chr6:g.157519972A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198838A>T , CM000668.2:g.157198838A>T	GRCh38
NC_000006.11:g.157519972A>T , CM000668.1:g.157519972A>T	GRCh37
NC_000006.10:g.157561664A>T	NCBI36
NG_032093.1:g.425909A>T
NG_032093.2:g.425909A>T
NG_066624.1:g.427813A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4251A>T	ENSP00000055163.8:p.Pro1417=
ENST00000414678.8:c.4320A>T	ENSP00000412835.3:p.Pro1440=
ENST00000637015.2:c.4539A>T	ENSP00000489729.2:p.Pro1513=
ENST00000346085.10:c.4290A>T	ENSP00000344546.5:p.Pro1430=
ENST00000350026.10:c.4002A>T	ENSP00000055163.7:p.Pro1334=
ENST00000414678.7:c.2568A>T	ENSP00000412835.2:p.Pro856=
ENST00000635849.1:c.1731A>T	ENSP00000490948.1:p.Pro577=
ENST00000635957.1:c.1362A>T	ENSP00000490385.1:p.Pro454=
ENST00000636227.1:n.2873A>T
ENST00000636254.1:n.330A>T
ENST00000636930.2:c.4410A>T MANE Select	ENSP00000490491.2:p.Pro1470=
ENST00000636940.1:n.2407A>T
ENST00000637015.1:c.1778A>T
ENST00000637568.1:c.1692A>T
ENST00000637741.1:n.1076A>T
ENST00000637810.1:c.1752A>T	ENSP00000489636.1:p.Pro584=
ENST00000637904.1:c.1911A>T	ENSP00000490550.1:p.Pro637=
ENST00000647938.1:c.4041A>T	ENSP00000498155.1:p.Pro1347=
ENST00000346085.9:c.4041A>T	ENSP00000344546.4:p.Pro1347=
ENST00000350026.9:c.4002A>T	ENSP00000055163.7:p.Pro1334=
ENST00000414678.6:c.2568A>T	ENSP00000412835.2:p.Pro856=
NM_017519.2:c.4002A>T	NP_059989.2:p.Pro1334=
NM_020732.3:c.4041A>T	NP_065783.3:p.Pro1347=
XM_005267069.3:c.4161A>T	XP_005267126.2:p.Pro1387=
XM_011535984.1:c.3240A>T	XP_011534286.1:p.Pro1080=
XM_011535985.1:c.3060A>T	XP_011534287.1:p.Pro1020=
XM_011535986.1:c.2820A>T	XP_011534288.1:p.Pro940=
XM_011535987.1:c.2439A>T	XP_011534289.1:p.Pro813=
XM_011535988.1:c.1302A>T	XP_011534290.1:p.Pro434=
NM_001346813.1:c.4161A>T	NP_001333742.1:p.Pro1387=
NM_001363725.1:c.1911A>T	NP_001350654.1:p.Pro637=
XM_011535984.2:c.4371A>T	XP_011534286.2:p.Pro1457=
XM_011535988.3:c.1302A>T	XP_011534290.1:p.Pro434=
XM_017011103.2:c.4272A>T	XP_016866592.1:p.Pro1424=
XM_017011104.1:c.4242A>T	XP_016866593.1:p.Pro1414=
XM_017011105.2:c.4212A>T	XP_016866594.1:p.Pro1404=
XM_017011106.2:c.4083A>T	XP_016866595.1:p.Pro1361=
XM_017011107.2:c.4062A>T	XP_016866596.1:p.Pro1354=
XR_002956289.1:n.4427-1867A>T
NM_001363725.2:c.1911A>T	NP_001350654.1:p.Pro637=
NM_001371656.1:c.4290A>T	NP_001358585.1:p.Pro1430=
NM_001374820.1:c.4290A>T	NP_001361749.1:p.Pro1430=
NM_001374828.1:c.4410A>T MANE Select	NP_001361757.1:p.Pro1470=
NM_017519.3:c.4251A>T	NP_059989.3:p.Pro1417=