Canonical Allele Identifier: CA366234568

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511172A>T (hg19) ; chr6:g.157190038A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190038A>T , CM000668.2:g.157190038A>T	GRCh38
NC_000006.11:g.157511172A>T , CM000668.1:g.157511172A>T	GRCh37
NC_000006.10:g.157552864A>T	NCBI36
NG_032093.1:g.417109A>T
NG_032093.2:g.417109A>T
NG_066624.1:g.419013A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900A>T	ENSP00000055163.8:p.Arg1300Ser
ENST00000414678.8:c.3969A>T	ENSP00000412835.3:p.Arg1323Ser
ENST00000637015.2:c.4188A>T	ENSP00000489729.2:p.Arg1396Ser
ENST00000346085.10:c.3939A>T	ENSP00000344546.5:p.Arg1313Ser
ENST00000350026.10:c.3651A>T	ENSP00000055163.7:p.Arg1217Ser
ENST00000414678.7:c.2217A>T	ENSP00000412835.2:p.Arg739Ser
ENST00000635849.1:c.1380A>T	ENSP00000490948.1:p.Arg460Ser
ENST00000635957.1:c.1014-3A>T	ENSP00000490385.1:n.1014-3A>T
ENST00000636930.2:c.4059A>T MANE Select	ENSP00000490491.2:p.Arg1353Ser
ENST00000636940.1:n.2056A>T
ENST00000637015.1:c.1427A>T
ENST00000637568.1:c.1341A>T
ENST00000637741.1:n.725A>T
ENST00000637810.1:c.1401A>T	ENSP00000489636.1:p.Arg467Ser
ENST00000637904.1:c.1560A>T	ENSP00000490550.1:p.Arg520Ser
ENST00000647938.1:c.3690A>T	ENSP00000498155.1:p.Arg1230Ser
ENST00000346085.9:c.3690A>T	ENSP00000344546.4:p.Arg1230Ser
ENST00000350026.9:c.3651A>T	ENSP00000055163.7:p.Arg1217Ser
ENST00000414678.6:c.2217A>T	ENSP00000412835.2:p.Arg739Ser
NM_017519.2:c.3651A>T	NP_059989.2:p.Arg1217Ser
NM_020732.3:c.3690A>T	NP_065783.3:p.Arg1230Ser
XM_005267069.3:c.3810A>T	XP_005267126.2:p.Arg1270Ser
XM_011535984.1:c.2889A>T	XP_011534286.1:p.Arg963Ser
XM_011535985.1:c.2709A>T	XP_011534287.1:p.Arg903Ser
XM_011535986.1:c.2469A>T	XP_011534288.1:p.Arg823Ser
XM_011535987.1:c.2088A>T	XP_011534289.1:p.Arg696Ser
XM_011535988.1:c.951A>T	XP_011534290.1:p.Arg317Ser
NM_001346813.1:c.3810A>T	NP_001333742.1:p.Arg1270Ser
NM_001363725.1:c.1560A>T	NP_001350654.1:p.Arg520Ser
XM_011535984.2:c.4020A>T	XP_011534286.2:p.Arg1340Ser
XM_011535988.3:c.951A>T	XP_011534290.1:p.Arg317Ser
XM_017011103.2:c.3921A>T	XP_016866592.1:p.Arg1307Ser
XM_017011104.1:c.3891A>T	XP_016866593.1:p.Arg1297Ser
XM_017011105.2:c.3861A>T	XP_016866594.1:p.Arg1287Ser
XM_017011106.2:c.3732A>T	XP_016866595.1:p.Arg1244Ser
XM_017011107.2:c.3711A>T	XP_016866596.1:p.Arg1237Ser
XR_002956289.1:n.4103A>T
NM_001363725.2:c.1560A>T	NP_001350654.1:p.Arg520Ser
NM_001371656.1:c.3939A>T	NP_001358585.1:p.Arg1313Ser
NM_001374820.1:c.3939A>T	NP_001361749.1:p.Arg1313Ser
NM_001374828.1:c.4059A>T MANE Select	NP_001361757.1:p.Arg1353Ser
NM_017519.3:c.3900A>T	NP_059989.3:p.Arg1300Ser