Canonical Allele Identifier: CA366227477

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502174A>C (hg19) ; chr6:g.157181040A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181040A>C , CM000668.2:g.157181040A>C	GRCh38
NC_000006.11:g.157502174A>C , CM000668.1:g.157502174A>C	GRCh37
NC_000006.10:g.157543866A>C	NCBI36
NG_032093.1:g.408111A>C
NG_032093.2:g.408111A>C
NG_066624.1:g.410015A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3417A>C	ENSP00000055163.8:p.Arg1139Ser
ENST00000414678.8:c.3486A>C	ENSP00000412835.3:p.Arg1162Ser
ENST00000637015.2:c.3705A>C	ENSP00000489729.2:p.Arg1235Ser
ENST00000319584.11:c.1590A>C	ENSP00000313006.7:p.Arg530Ser
ENST00000346085.10:c.3456A>C	ENSP00000344546.5:p.Arg1152Ser
ENST00000350026.10:c.3168A>C	ENSP00000055163.7:p.Arg1056Ser
ENST00000414678.7:c.1734A>C	ENSP00000412835.2:p.Arg578Ser
ENST00000635849.1:c.897A>C	ENSP00000490948.1:p.Arg299Ser
ENST00000635957.1:c.531A>C	ENSP00000490385.1:p.Arg177Ser
ENST00000636930.2:c.3576A>C MANE Select	ENSP00000490491.2:p.Arg1192Ser
ENST00000636940.1:n.1573A>C
ENST00000637015.1:c.944A>C
ENST00000637568.1:c.858A>C
ENST00000637741.1:n.242A>C
ENST00000637810.1:c.918A>C	ENSP00000489636.1:p.Arg306Ser
ENST00000637904.1:c.1077A>C	ENSP00000490550.1:p.Arg359Ser
ENST00000647938.1:c.3207A>C	ENSP00000498155.1:p.Arg1069Ser
ENST00000319584.10:c.1593A>C	ENSP00000313006.6:p.Arg531Ser
ENST00000346085.9:c.3207A>C	ENSP00000344546.4:p.Arg1069Ser
ENST00000350026.9:c.3168A>C	ENSP00000055163.7:p.Arg1056Ser
ENST00000400790.3:c.369A>C	ENSP00000383596.3:p.Arg123Ser
ENST00000414678.6:c.1734A>C	ENSP00000412835.2:p.Arg578Ser
ENST00000478761.3:c.778A>C
NM_017519.2:c.3168A>C	NP_059989.2:p.Arg1056Ser
NM_020732.3:c.3207A>C	NP_065783.3:p.Arg1069Ser
XM_005267069.3:c.3327A>C	XP_005267126.2:p.Arg1109Ser
XM_011535984.1:c.2406A>C	XP_011534286.1:p.Arg802Ser
XM_011535985.1:c.2226A>C	XP_011534287.1:p.Arg742Ser
XM_011535986.1:c.1986A>C	XP_011534288.1:p.Arg662Ser
XM_011535987.1:c.1605A>C	XP_011534289.1:p.Arg535Ser
XM_011535988.1:c.468A>C	XP_011534290.1:p.Arg156Ser
NM_001346813.1:c.3327A>C	NP_001333742.1:p.Arg1109Ser
NM_001363725.1:c.1077A>C	NP_001350654.1:p.Arg359Ser
XM_011535984.2:c.3537A>C	XP_011534286.2:p.Arg1179Ser
XM_011535988.3:c.468A>C	XP_011534290.1:p.Arg156Ser
XM_017011103.2:c.3438A>C	XP_016866592.1:p.Arg1146Ser
XM_017011104.1:c.3408A>C	XP_016866593.1:p.Arg1136Ser
XM_017011105.2:c.3378A>C	XP_016866594.1:p.Arg1126Ser
XM_017011106.2:c.3249A>C	XP_016866595.1:p.Arg1083Ser
XM_017011107.2:c.3228A>C	XP_016866596.1:p.Arg1076Ser
XR_002956289.1:n.3620A>C
NM_001363725.2:c.1077A>C	NP_001350654.1:p.Arg359Ser
NM_001371656.1:c.3456A>C	NP_001358585.1:p.Arg1152Ser
NM_001374820.1:c.3456A>C	NP_001361749.1:p.Arg1152Ser
NM_001374828.1:c.3576A>C MANE Select	NP_001361757.1:p.Arg1192Ser
NM_017519.3:c.3417A>C	NP_059989.3:p.Arg1139Ser