Canonical Allele Identifier: CA366241827

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522207G>C (hg19) ; chr6:g.157201073G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201073G>C , CM000668.2:g.157201073G>C	GRCh38
NC_000006.11:g.157522207G>C , CM000668.1:g.157522207G>C	GRCh37
NC_000006.10:g.157563899G>C	NCBI36
NG_032093.1:g.428144G>C
NG_032093.2:g.428144G>C
NG_066624.1:g.430048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4689G>C	ENSP00000055163.8:p.Met1563Ile
ENST00000414678.8:c.4758G>C	ENSP00000412835.3:p.Met1586Ile
ENST00000637015.2:c.4977G>C	ENSP00000489729.2:p.Met1659Ile
ENST00000346085.10:c.4728G>C	ENSP00000344546.5:p.Met1576Ile
ENST00000350026.10:c.4440G>C	ENSP00000055163.7:p.Met1480Ile
ENST00000414678.7:c.3006G>C	ENSP00000412835.2:p.Met1002Ile
ENST00000635849.1:c.2169G>C	ENSP00000490948.1:p.Met723Ile
ENST00000635957.1:c.1800G>C	ENSP00000490385.1:p.Met600Ile
ENST00000636227.1:n.3311G>C
ENST00000636254.1:n.768G>C
ENST00000636930.2:c.4848G>C MANE Select	ENSP00000490491.2:p.Met1616Ile
ENST00000636940.1:n.2845G>C
ENST00000637015.1:c.2216G>C
ENST00000637568.1:c.2130G>C
ENST00000637741.1:n.1514G>C
ENST00000637810.1:c.2190G>C	ENSP00000489636.1:p.Met730Ile
ENST00000637904.1:c.2349G>C	ENSP00000490550.1:p.Met783Ile
ENST00000647938.1:c.4479G>C	ENSP00000498155.1:p.Met1493Ile
ENST00000346085.9:c.4479G>C	ENSP00000344546.4:p.Met1493Ile
ENST00000350026.9:c.4440G>C	ENSP00000055163.7:p.Met1480Ile
ENST00000414678.6:c.3006G>C	ENSP00000412835.2:p.Met1002Ile
NM_017519.2:c.4440G>C	NP_059989.2:p.Met1480Ile
NM_020732.3:c.4479G>C	NP_065783.3:p.Met1493Ile
XM_005267069.3:c.4599G>C	XP_005267126.2:p.Met1533Ile
XM_011535984.1:c.3678G>C	XP_011534286.1:p.Met1226Ile
XM_011535985.1:c.3498G>C	XP_011534287.1:p.Met1166Ile
XM_011535986.1:c.3258G>C	XP_011534288.1:p.Met1086Ile
XM_011535987.1:c.2877G>C	XP_011534289.1:p.Met959Ile
XM_011535988.1:c.1740G>C	XP_011534290.1:p.Met580Ile
NM_001346813.1:c.4599G>C	NP_001333742.1:p.Met1533Ile
NM_001363725.1:c.2349G>C	NP_001350654.1:p.Met783Ile
XM_011535984.2:c.4809G>C	XP_011534286.2:p.Met1603Ile
XM_011535988.3:c.1740G>C	XP_011534290.1:p.Met580Ile
XM_017011103.2:c.4710G>C	XP_016866592.1:p.Met1570Ile
XM_017011104.1:c.4680G>C	XP_016866593.1:p.Met1560Ile
XM_017011105.2:c.4650G>C	XP_016866594.1:p.Met1550Ile
XM_017011106.2:c.4521G>C	XP_016866595.1:p.Met1507Ile
XM_017011107.2:c.4500G>C	XP_016866596.1:p.Met1500Ile
XR_002956289.1:n.4795G>C
NM_001363725.2:c.2349G>C	NP_001350654.1:p.Met783Ile
NM_001371656.1:c.4728G>C	NP_001358585.1:p.Met1576Ile
NM_001374820.1:c.4728G>C	NP_001361749.1:p.Met1576Ile
NM_001374828.1:c.4848G>C MANE Select	NP_001361757.1:p.Met1616Ile
NM_017519.3:c.4689G>C	NP_059989.3:p.Met1563Ile