Canonical Allele Identifier: CA366234085

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510820G>T (hg19) ; chr6:g.157189686G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189686G>T , CM000668.2:g.157189686G>T	GRCh38
NC_000006.11:g.157510820G>T , CM000668.1:g.157510820G>T	GRCh37
NC_000006.10:g.157552512G>T	NCBI36
NG_032093.1:g.416757G>T
NG_032093.2:g.416757G>T
NG_066624.1:g.418661G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3805G>T	ENSP00000055163.8:p.Gly1269Cys
ENST00000414678.8:c.3874G>T	ENSP00000412835.3:p.Gly1292Cys
ENST00000637015.2:c.4093G>T	ENSP00000489729.2:p.Gly1365Cys
ENST00000346085.10:c.3844G>T	ENSP00000344546.5:p.Gly1282Cys
ENST00000350026.10:c.3556G>T	ENSP00000055163.7:p.Gly1186Cys
ENST00000414678.7:c.2122G>T	ENSP00000412835.2:p.Gly708Cys
ENST00000635849.1:c.1285G>T	ENSP00000490948.1:p.Gly429Cys
ENST00000635957.1:c.919G>T	ENSP00000490385.1:p.Gly307Cys
ENST00000636930.2:c.3964G>T MANE Select	ENSP00000490491.2:p.Gly1322Cys
ENST00000636940.1:n.1961G>T
ENST00000637015.1:c.1332G>T
ENST00000637568.1:c.1246G>T
ENST00000637741.1:n.630G>T
ENST00000637810.1:c.1306G>T	ENSP00000489636.1:p.Gly436Cys
ENST00000637904.1:c.1465G>T	ENSP00000490550.1:p.Gly489Cys
ENST00000647938.1:c.3595G>T	ENSP00000498155.1:p.Gly1199Cys
ENST00000346085.9:c.3595G>T	ENSP00000344546.4:p.Gly1199Cys
ENST00000350026.9:c.3556G>T	ENSP00000055163.7:p.Gly1186Cys
ENST00000414678.6:c.2122G>T	ENSP00000412835.2:p.Gly708Cys
NM_017519.2:c.3556G>T	NP_059989.2:p.Gly1186Cys
NM_020732.3:c.3595G>T	NP_065783.3:p.Gly1199Cys
XM_005267069.3:c.3715G>T	XP_005267126.2:p.Gly1239Cys
XM_011535984.1:c.2794G>T	XP_011534286.1:p.Gly932Cys
XM_011535985.1:c.2614G>T	XP_011534287.1:p.Gly872Cys
XM_011535986.1:c.2374G>T	XP_011534288.1:p.Gly792Cys
XM_011535987.1:c.1993G>T	XP_011534289.1:p.Gly665Cys
XM_011535988.1:c.856G>T	XP_011534290.1:p.Gly286Cys
NM_001346813.1:c.3715G>T	NP_001333742.1:p.Gly1239Cys
NM_001363725.1:c.1465G>T	NP_001350654.1:p.Gly489Cys
XM_011535984.2:c.3925G>T	XP_011534286.2:p.Gly1309Cys
XM_011535988.3:c.856G>T	XP_011534290.1:p.Gly286Cys
XM_017011103.2:c.3826G>T	XP_016866592.1:p.Gly1276Cys
XM_017011104.1:c.3796G>T	XP_016866593.1:p.Gly1266Cys
XM_017011105.2:c.3766G>T	XP_016866594.1:p.Gly1256Cys
XM_017011106.2:c.3637G>T	XP_016866595.1:p.Gly1213Cys
XM_017011107.2:c.3616G>T	XP_016866596.1:p.Gly1206Cys
XR_002956289.1:n.4008G>T
NM_001363725.2:c.1465G>T	NP_001350654.1:p.Gly489Cys
NM_001371656.1:c.3844G>T	NP_001358585.1:p.Gly1282Cys
NM_001374820.1:c.3844G>T	NP_001361749.1:p.Gly1282Cys
NM_001374828.1:c.3964G>T MANE Select	NP_001361757.1:p.Gly1322Cys
NM_017519.3:c.3805G>T	NP_059989.3:p.Gly1269Cys