Canonical Allele Identifier: CA366234084

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3805G>C	ENSP00000055163.8:p.Gly1269Arg
ENST00000414678.8:c.3874G>C	ENSP00000412835.3:p.Gly1292Arg
ENST00000637015.2:c.4093G>C	ENSP00000489729.2:p.Gly1365Arg
ENST00000346085.10:c.3844G>C	ENSP00000344546.5:p.Gly1282Arg
ENST00000350026.10:c.3556G>C	ENSP00000055163.7:p.Gly1186Arg
ENST00000414678.7:c.2122G>C	ENSP00000412835.2:p.Gly708Arg
ENST00000635849.1:c.1285G>C	ENSP00000490948.1:p.Gly429Arg
ENST00000635957.1:c.919G>C	ENSP00000490385.1:p.Gly307Arg
ENST00000636930.2:c.3964G>C MANE Select	ENSP00000490491.2:p.Gly1322Arg
ENST00000636940.1:n.1961G>C
ENST00000637015.1:c.1332G>C
ENST00000637568.1:c.1246G>C
ENST00000637741.1:n.630G>C
ENST00000637810.1:c.1306G>C	ENSP00000489636.1:p.Gly436Arg
ENST00000637904.1:c.1465G>C	ENSP00000490550.1:p.Gly489Arg
ENST00000647938.1:c.3595G>C	ENSP00000498155.1:p.Gly1199Arg
ENST00000346085.9:c.3595G>C	ENSP00000344546.4:p.Gly1199Arg
ENST00000350026.9:c.3556G>C	ENSP00000055163.7:p.Gly1186Arg
ENST00000414678.6:c.2122G>C	ENSP00000412835.2:p.Gly708Arg
NM_017519.2:c.3556G>C	NP_059989.2:p.Gly1186Arg
NM_020732.3:c.3595G>C	NP_065783.3:p.Gly1199Arg
XM_005267069.3:c.3715G>C	XP_005267126.2:p.Gly1239Arg
XM_011535984.1:c.2794G>C	XP_011534286.1:p.Gly932Arg
XM_011535985.1:c.2614G>C	XP_011534287.1:p.Gly872Arg
XM_011535986.1:c.2374G>C	XP_011534288.1:p.Gly792Arg
XM_011535987.1:c.1993G>C	XP_011534289.1:p.Gly665Arg
XM_011535988.1:c.856G>C	XP_011534290.1:p.Gly286Arg
NM_001346813.1:c.3715G>C	NP_001333742.1:p.Gly1239Arg
NM_001363725.1:c.1465G>C	NP_001350654.1:p.Gly489Arg
XM_011535984.2:c.3925G>C	XP_011534286.2:p.Gly1309Arg
XM_011535988.3:c.856G>C	XP_011534290.1:p.Gly286Arg
XM_017011103.2:c.3826G>C	XP_016866592.1:p.Gly1276Arg
XM_017011104.1:c.3796G>C	XP_016866593.1:p.Gly1266Arg
XM_017011105.2:c.3766G>C	XP_016866594.1:p.Gly1256Arg
XM_017011106.2:c.3637G>C	XP_016866595.1:p.Gly1213Arg
XM_017011107.2:c.3616G>C	XP_016866596.1:p.Gly1206Arg
XR_002956289.1:n.4008G>C
NM_001363725.2:c.1465G>C	NP_001350654.1:p.Gly489Arg
NM_001371656.1:c.3844G>C	NP_001358585.1:p.Gly1282Arg
NM_001374820.1:c.3844G>C	NP_001361749.1:p.Gly1282Arg
NM_001374828.1:c.3964G>C MANE Select	NP_001361757.1:p.Gly1322Arg
NM_017519.3:c.3805G>C	NP_059989.3:p.Gly1269Arg