Canonical Allele Identifier: CA366234055

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510805A>T (hg19) ; chr6:g.157189671A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189671A>T , CM000668.2:g.157189671A>T	GRCh38
NC_000006.11:g.157510805A>T , CM000668.1:g.157510805A>T	GRCh37
NC_000006.10:g.157552497A>T	NCBI36
NG_032093.1:g.416742A>T
NG_032093.2:g.416742A>T
NG_066624.1:g.418646A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3790A>T	ENSP00000055163.8:p.Thr1264Ser
ENST00000414678.8:c.3859A>T	ENSP00000412835.3:p.Thr1287Ser
ENST00000637015.2:c.4078A>T	ENSP00000489729.2:p.Thr1360Ser
ENST00000346085.10:c.3829A>T	ENSP00000344546.5:p.Thr1277Ser
ENST00000350026.10:c.3541A>T	ENSP00000055163.7:p.Thr1181Ser
ENST00000414678.7:c.2107A>T	ENSP00000412835.2:p.Thr703Ser
ENST00000635849.1:c.1270A>T	ENSP00000490948.1:p.Thr424Ser
ENST00000635957.1:c.904A>T	ENSP00000490385.1:p.Thr302Ser
ENST00000636930.2:c.3949A>T MANE Select	ENSP00000490491.2:p.Thr1317Ser
ENST00000636940.1:n.1946A>T
ENST00000637015.1:c.1317A>T
ENST00000637568.1:c.1231A>T
ENST00000637741.1:n.615A>T
ENST00000637810.1:c.1291A>T	ENSP00000489636.1:p.Thr431Ser
ENST00000637904.1:c.1450A>T	ENSP00000490550.1:p.Thr484Ser
ENST00000647938.1:c.3580A>T	ENSP00000498155.1:p.Thr1194Ser
ENST00000346085.9:c.3580A>T	ENSP00000344546.4:p.Thr1194Ser
ENST00000350026.9:c.3541A>T	ENSP00000055163.7:p.Thr1181Ser
ENST00000414678.6:c.2107A>T	ENSP00000412835.2:p.Thr703Ser
NM_017519.2:c.3541A>T	NP_059989.2:p.Thr1181Ser
NM_020732.3:c.3580A>T	NP_065783.3:p.Thr1194Ser
XM_005267069.3:c.3700A>T	XP_005267126.2:p.Thr1234Ser
XM_011535984.1:c.2779A>T	XP_011534286.1:p.Thr927Ser
XM_011535985.1:c.2599A>T	XP_011534287.1:p.Thr867Ser
XM_011535986.1:c.2359A>T	XP_011534288.1:p.Thr787Ser
XM_011535987.1:c.1978A>T	XP_011534289.1:p.Thr660Ser
XM_011535988.1:c.841A>T	XP_011534290.1:p.Thr281Ser
NM_001346813.1:c.3700A>T	NP_001333742.1:p.Thr1234Ser
NM_001363725.1:c.1450A>T	NP_001350654.1:p.Thr484Ser
XM_011535984.2:c.3910A>T	XP_011534286.2:p.Thr1304Ser
XM_011535988.3:c.841A>T	XP_011534290.1:p.Thr281Ser
XM_017011103.2:c.3811A>T	XP_016866592.1:p.Thr1271Ser
XM_017011104.1:c.3781A>T	XP_016866593.1:p.Thr1261Ser
XM_017011105.2:c.3751A>T	XP_016866594.1:p.Thr1251Ser
XM_017011106.2:c.3622A>T	XP_016866595.1:p.Thr1208Ser
XM_017011107.2:c.3601A>T	XP_016866596.1:p.Thr1201Ser
XR_002956289.1:n.3993A>T
NM_001363725.2:c.1450A>T	NP_001350654.1:p.Thr484Ser
NM_001371656.1:c.3829A>T	NP_001358585.1:p.Thr1277Ser
NM_001374820.1:c.3829A>T	NP_001361749.1:p.Thr1277Ser
NM_001374828.1:c.3949A>T MANE Select	NP_001361757.1:p.Thr1317Ser
NM_017519.3:c.3790A>T	NP_059989.3:p.Thr1264Ser