Canonical Allele Identifier: CA366234119

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510835G>C (hg19) ; chr6:g.157189701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189701G>C , CM000668.2:g.157189701G>C	GRCh38
NC_000006.11:g.157510835G>C , CM000668.1:g.157510835G>C	GRCh37
NC_000006.10:g.157552527G>C	NCBI36
NG_032093.1:g.416772G>C
NG_032093.2:g.416772G>C
NG_066624.1:g.418676G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3820G>C	ENSP00000055163.8:p.Ala1274Pro
ENST00000414678.8:c.3889G>C	ENSP00000412835.3:p.Ala1297Pro
ENST00000637015.2:c.4108G>C	ENSP00000489729.2:p.Ala1370Pro
ENST00000346085.10:c.3859G>C	ENSP00000344546.5:p.Ala1287Pro
ENST00000350026.10:c.3571G>C	ENSP00000055163.7:p.Ala1191Pro
ENST00000414678.7:c.2137G>C	ENSP00000412835.2:p.Ala713Pro
ENST00000635849.1:c.1300G>C	ENSP00000490948.1:p.Ala434Pro
ENST00000635957.1:c.934G>C	ENSP00000490385.1:p.Ala312Pro
ENST00000636930.2:c.3979G>C MANE Select	ENSP00000490491.2:p.Ala1327Pro
ENST00000636940.1:n.1976G>C
ENST00000637015.1:c.1347G>C
ENST00000637568.1:c.1261G>C
ENST00000637741.1:n.645G>C
ENST00000637810.1:c.1321G>C	ENSP00000489636.1:p.Ala441Pro
ENST00000637904.1:c.1480G>C	ENSP00000490550.1:p.Ala494Pro
ENST00000647938.1:c.3610G>C	ENSP00000498155.1:p.Ala1204Pro
ENST00000346085.9:c.3610G>C	ENSP00000344546.4:p.Ala1204Pro
ENST00000350026.9:c.3571G>C	ENSP00000055163.7:p.Ala1191Pro
ENST00000414678.6:c.2137G>C	ENSP00000412835.2:p.Ala713Pro
NM_017519.2:c.3571G>C	NP_059989.2:p.Ala1191Pro
NM_020732.3:c.3610G>C	NP_065783.3:p.Ala1204Pro
XM_005267069.3:c.3730G>C	XP_005267126.2:p.Ala1244Pro
XM_011535984.1:c.2809G>C	XP_011534286.1:p.Ala937Pro
XM_011535985.1:c.2629G>C	XP_011534287.1:p.Ala877Pro
XM_011535986.1:c.2389G>C	XP_011534288.1:p.Ala797Pro
XM_011535987.1:c.2008G>C	XP_011534289.1:p.Ala670Pro
XM_011535988.1:c.871G>C	XP_011534290.1:p.Ala291Pro
NM_001346813.1:c.3730G>C	NP_001333742.1:p.Ala1244Pro
NM_001363725.1:c.1480G>C	NP_001350654.1:p.Ala494Pro
XM_011535984.2:c.3940G>C	XP_011534286.2:p.Ala1314Pro
XM_011535988.3:c.871G>C	XP_011534290.1:p.Ala291Pro
XM_017011103.2:c.3841G>C	XP_016866592.1:p.Ala1281Pro
XM_017011104.1:c.3811G>C	XP_016866593.1:p.Ala1271Pro
XM_017011105.2:c.3781G>C	XP_016866594.1:p.Ala1261Pro
XM_017011106.2:c.3652G>C	XP_016866595.1:p.Ala1218Pro
XM_017011107.2:c.3631G>C	XP_016866596.1:p.Ala1211Pro
XR_002956289.1:n.4023G>C
NM_001363725.2:c.1480G>C	NP_001350654.1:p.Ala494Pro
NM_001371656.1:c.3859G>C	NP_001358585.1:p.Ala1287Pro
NM_001374820.1:c.3859G>C	NP_001361749.1:p.Ala1287Pro
NM_001374828.1:c.3979G>C MANE Select	NP_001361757.1:p.Ala1327Pro
NM_017519.3:c.3820G>C	NP_059989.3:p.Ala1274Pro