Canonical Allele Identifier: CA366234131

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510840G>C (hg19) ; chr6:g.157189706G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189706G>C , CM000668.2:g.157189706G>C	GRCh38
NC_000006.11:g.157510840G>C , CM000668.1:g.157510840G>C	GRCh37
NC_000006.10:g.157552532G>C	NCBI36
NG_032093.1:g.416777G>C
NG_032093.2:g.416777G>C
NG_066624.1:g.418681G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3825G>C	ENSP00000055163.8:p.Glu1275Asp
ENST00000414678.8:c.3894G>C	ENSP00000412835.3:p.Glu1298Asp
ENST00000637015.2:c.4113G>C	ENSP00000489729.2:p.Glu1371Asp
ENST00000346085.10:c.3864G>C	ENSP00000344546.5:p.Glu1288Asp
ENST00000350026.10:c.3576G>C	ENSP00000055163.7:p.Glu1192Asp
ENST00000414678.7:c.2142G>C	ENSP00000412835.2:p.Glu714Asp
ENST00000635849.1:c.1305G>C	ENSP00000490948.1:p.Glu435Asp
ENST00000635957.1:c.939G>C	ENSP00000490385.1:p.Glu313Asp
ENST00000636930.2:c.3984G>C MANE Select	ENSP00000490491.2:p.Glu1328Asp
ENST00000636940.1:n.1981G>C
ENST00000637015.1:c.1352G>C
ENST00000637568.1:c.1266G>C
ENST00000637741.1:n.650G>C
ENST00000637810.1:c.1326G>C	ENSP00000489636.1:p.Glu442Asp
ENST00000637904.1:c.1485G>C	ENSP00000490550.1:p.Glu495Asp
ENST00000647938.1:c.3615G>C	ENSP00000498155.1:p.Glu1205Asp
ENST00000346085.9:c.3615G>C	ENSP00000344546.4:p.Glu1205Asp
ENST00000350026.9:c.3576G>C	ENSP00000055163.7:p.Glu1192Asp
ENST00000414678.6:c.2142G>C	ENSP00000412835.2:p.Glu714Asp
NM_017519.2:c.3576G>C	NP_059989.2:p.Glu1192Asp
NM_020732.3:c.3615G>C	NP_065783.3:p.Glu1205Asp
XM_005267069.3:c.3735G>C	XP_005267126.2:p.Glu1245Asp
XM_011535984.1:c.2814G>C	XP_011534286.1:p.Glu938Asp
XM_011535985.1:c.2634G>C	XP_011534287.1:p.Glu878Asp
XM_011535986.1:c.2394G>C	XP_011534288.1:p.Glu798Asp
XM_011535987.1:c.2013G>C	XP_011534289.1:p.Glu671Asp
XM_011535988.1:c.876G>C	XP_011534290.1:p.Glu292Asp
NM_001346813.1:c.3735G>C	NP_001333742.1:p.Glu1245Asp
NM_001363725.1:c.1485G>C	NP_001350654.1:p.Glu495Asp
XM_011535984.2:c.3945G>C	XP_011534286.2:p.Glu1315Asp
XM_011535988.3:c.876G>C	XP_011534290.1:p.Glu292Asp
XM_017011103.2:c.3846G>C	XP_016866592.1:p.Glu1282Asp
XM_017011104.1:c.3816G>C	XP_016866593.1:p.Glu1272Asp
XM_017011105.2:c.3786G>C	XP_016866594.1:p.Glu1262Asp
XM_017011106.2:c.3657G>C	XP_016866595.1:p.Glu1219Asp
XM_017011107.2:c.3636G>C	XP_016866596.1:p.Glu1212Asp
XR_002956289.1:n.4028G>C
NM_001363725.2:c.1485G>C	NP_001350654.1:p.Glu495Asp
NM_001371656.1:c.3864G>C	NP_001358585.1:p.Glu1288Asp
NM_001374820.1:c.3864G>C	NP_001361749.1:p.Glu1288Asp
NM_001374828.1:c.3984G>C MANE Select	NP_001361757.1:p.Glu1328Asp
NM_017519.3:c.3825G>C	NP_059989.3:p.Glu1275Asp