Canonical Allele Identifier: CA366234092

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3809G>C	ENSP00000055163.8:p.Ser1270Thr
ENST00000414678.8:c.3878G>C	ENSP00000412835.3:p.Ser1293Thr
ENST00000637015.2:c.4097G>C	ENSP00000489729.2:p.Ser1366Thr
ENST00000346085.10:c.3848G>C	ENSP00000344546.5:p.Ser1283Thr
ENST00000350026.10:c.3560G>C	ENSP00000055163.7:p.Ser1187Thr
ENST00000414678.7:c.2126G>C	ENSP00000412835.2:p.Ser709Thr
ENST00000635849.1:c.1289G>C	ENSP00000490948.1:p.Ser430Thr
ENST00000635957.1:c.923G>C	ENSP00000490385.1:p.Ser308Thr
ENST00000636930.2:c.3968G>C MANE Select	ENSP00000490491.2:p.Ser1323Thr
ENST00000636940.1:n.1965G>C
ENST00000637015.1:c.1336G>C
ENST00000637568.1:c.1250G>C
ENST00000637741.1:n.634G>C
ENST00000637810.1:c.1310G>C	ENSP00000489636.1:p.Ser437Thr
ENST00000637904.1:c.1469G>C	ENSP00000490550.1:p.Ser490Thr
ENST00000647938.1:c.3599G>C	ENSP00000498155.1:p.Ser1200Thr
ENST00000346085.9:c.3599G>C	ENSP00000344546.4:p.Ser1200Thr
ENST00000350026.9:c.3560G>C	ENSP00000055163.7:p.Ser1187Thr
ENST00000414678.6:c.2126G>C	ENSP00000412835.2:p.Ser709Thr
NM_017519.2:c.3560G>C	NP_059989.2:p.Ser1187Thr
NM_020732.3:c.3599G>C	NP_065783.3:p.Ser1200Thr
XM_005267069.3:c.3719G>C	XP_005267126.2:p.Ser1240Thr
XM_011535984.1:c.2798G>C	XP_011534286.1:p.Ser933Thr
XM_011535985.1:c.2618G>C	XP_011534287.1:p.Ser873Thr
XM_011535986.1:c.2378G>C	XP_011534288.1:p.Ser793Thr
XM_011535987.1:c.1997G>C	XP_011534289.1:p.Ser666Thr
XM_011535988.1:c.860G>C	XP_011534290.1:p.Ser287Thr
NM_001346813.1:c.3719G>C	NP_001333742.1:p.Ser1240Thr
NM_001363725.1:c.1469G>C	NP_001350654.1:p.Ser490Thr
XM_011535984.2:c.3929G>C	XP_011534286.2:p.Ser1310Thr
XM_011535988.3:c.860G>C	XP_011534290.1:p.Ser287Thr
XM_017011103.2:c.3830G>C	XP_016866592.1:p.Ser1277Thr
XM_017011104.1:c.3800G>C	XP_016866593.1:p.Ser1267Thr
XM_017011105.2:c.3770G>C	XP_016866594.1:p.Ser1257Thr
XM_017011106.2:c.3641G>C	XP_016866595.1:p.Ser1214Thr
XM_017011107.2:c.3620G>C	XP_016866596.1:p.Ser1207Thr
XR_002956289.1:n.4012G>C
NM_001363725.2:c.1469G>C	NP_001350654.1:p.Ser490Thr
NM_001371656.1:c.3848G>C	NP_001358585.1:p.Ser1283Thr
NM_001374820.1:c.3848G>C	NP_001361749.1:p.Ser1283Thr
NM_001374828.1:c.3968G>C MANE Select	NP_001361757.1:p.Ser1323Thr
NM_017519.3:c.3809G>C	NP_059989.3:p.Ser1270Thr