Canonical Allele Identifier: CA366234093

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510824G>T (hg19) ; chr6:g.157189690G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189690G>T , CM000668.2:g.157189690G>T	GRCh38
NC_000006.11:g.157510824G>T , CM000668.1:g.157510824G>T	GRCh37
NC_000006.10:g.157552516G>T	NCBI36
NG_032093.1:g.416761G>T
NG_032093.2:g.416761G>T
NG_066624.1:g.418665G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3809G>T	ENSP00000055163.8:p.Ser1270Ile
ENST00000414678.8:c.3878G>T	ENSP00000412835.3:p.Ser1293Ile
ENST00000637015.2:c.4097G>T	ENSP00000489729.2:p.Ser1366Ile
ENST00000346085.10:c.3848G>T	ENSP00000344546.5:p.Ser1283Ile
ENST00000350026.10:c.3560G>T	ENSP00000055163.7:p.Ser1187Ile
ENST00000414678.7:c.2126G>T	ENSP00000412835.2:p.Ser709Ile
ENST00000635849.1:c.1289G>T	ENSP00000490948.1:p.Ser430Ile
ENST00000635957.1:c.923G>T	ENSP00000490385.1:p.Ser308Ile
ENST00000636930.2:c.3968G>T MANE Select	ENSP00000490491.2:p.Ser1323Ile
ENST00000636940.1:n.1965G>T
ENST00000637015.1:c.1336G>T
ENST00000637568.1:c.1250G>T
ENST00000637741.1:n.634G>T
ENST00000637810.1:c.1310G>T	ENSP00000489636.1:p.Ser437Ile
ENST00000637904.1:c.1469G>T	ENSP00000490550.1:p.Ser490Ile
ENST00000647938.1:c.3599G>T	ENSP00000498155.1:p.Ser1200Ile
ENST00000346085.9:c.3599G>T	ENSP00000344546.4:p.Ser1200Ile
ENST00000350026.9:c.3560G>T	ENSP00000055163.7:p.Ser1187Ile
ENST00000414678.6:c.2126G>T	ENSP00000412835.2:p.Ser709Ile
NM_017519.2:c.3560G>T	NP_059989.2:p.Ser1187Ile
NM_020732.3:c.3599G>T	NP_065783.3:p.Ser1200Ile
XM_005267069.3:c.3719G>T	XP_005267126.2:p.Ser1240Ile
XM_011535984.1:c.2798G>T	XP_011534286.1:p.Ser933Ile
XM_011535985.1:c.2618G>T	XP_011534287.1:p.Ser873Ile
XM_011535986.1:c.2378G>T	XP_011534288.1:p.Ser793Ile
XM_011535987.1:c.1997G>T	XP_011534289.1:p.Ser666Ile
XM_011535988.1:c.860G>T	XP_011534290.1:p.Ser287Ile
NM_001346813.1:c.3719G>T	NP_001333742.1:p.Ser1240Ile
NM_001363725.1:c.1469G>T	NP_001350654.1:p.Ser490Ile
XM_011535984.2:c.3929G>T	XP_011534286.2:p.Ser1310Ile
XM_011535988.3:c.860G>T	XP_011534290.1:p.Ser287Ile
XM_017011103.2:c.3830G>T	XP_016866592.1:p.Ser1277Ile
XM_017011104.1:c.3800G>T	XP_016866593.1:p.Ser1267Ile
XM_017011105.2:c.3770G>T	XP_016866594.1:p.Ser1257Ile
XM_017011106.2:c.3641G>T	XP_016866595.1:p.Ser1214Ile
XM_017011107.2:c.3620G>T	XP_016866596.1:p.Ser1207Ile
XR_002956289.1:n.4012G>T
NM_001363725.2:c.1469G>T	NP_001350654.1:p.Ser490Ile
NM_001371656.1:c.3848G>T	NP_001358585.1:p.Ser1283Ile
NM_001374820.1:c.3848G>T	NP_001361749.1:p.Ser1283Ile
NM_001374828.1:c.3968G>T MANE Select	NP_001361757.1:p.Ser1323Ile
NM_017519.3:c.3809G>T	NP_059989.3:p.Ser1270Ile