Canonical Allele Identifier: CA366234047

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510802C>G (hg19) ; chr6:g.157189668C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189668C>G , CM000668.2:g.157189668C>G	GRCh38
NC_000006.11:g.157510802C>G , CM000668.1:g.157510802C>G	GRCh37
NC_000006.10:g.157552494C>G	NCBI36
NG_032093.1:g.416739C>G
NG_032093.2:g.416739C>G
NG_066624.1:g.418643C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3787C>G	ENSP00000055163.8:p.Gln1263Glu
ENST00000414678.8:c.3856C>G	ENSP00000412835.3:p.Gln1286Glu
ENST00000637015.2:c.4075C>G	ENSP00000489729.2:p.Gln1359Glu
ENST00000346085.10:c.3826C>G	ENSP00000344546.5:p.Gln1276Glu
ENST00000350026.10:c.3538C>G	ENSP00000055163.7:p.Gln1180Glu
ENST00000414678.7:c.2104C>G	ENSP00000412835.2:p.Gln702Glu
ENST00000635849.1:c.1267C>G	ENSP00000490948.1:p.Gln423Glu
ENST00000635957.1:c.901C>G	ENSP00000490385.1:p.Gln301Glu
ENST00000636930.2:c.3946C>G MANE Select	ENSP00000490491.2:p.Gln1316Glu
ENST00000636940.1:n.1943C>G
ENST00000637015.1:c.1314C>G
ENST00000637568.1:c.1228C>G
ENST00000637741.1:n.612C>G
ENST00000637810.1:c.1288C>G	ENSP00000489636.1:p.Gln430Glu
ENST00000637904.1:c.1447C>G	ENSP00000490550.1:p.Gln483Glu
ENST00000647938.1:c.3577C>G	ENSP00000498155.1:p.Gln1193Glu
ENST00000346085.9:c.3577C>G	ENSP00000344546.4:p.Gln1193Glu
ENST00000350026.9:c.3538C>G	ENSP00000055163.7:p.Gln1180Glu
ENST00000414678.6:c.2104C>G	ENSP00000412835.2:p.Gln702Glu
NM_017519.2:c.3538C>G	NP_059989.2:p.Gln1180Glu
NM_020732.3:c.3577C>G	NP_065783.3:p.Gln1193Glu
XM_005267069.3:c.3697C>G	XP_005267126.2:p.Gln1233Glu
XM_011535984.1:c.2776C>G	XP_011534286.1:p.Gln926Glu
XM_011535985.1:c.2596C>G	XP_011534287.1:p.Gln866Glu
XM_011535986.1:c.2356C>G	XP_011534288.1:p.Gln786Glu
XM_011535987.1:c.1975C>G	XP_011534289.1:p.Gln659Glu
XM_011535988.1:c.838C>G	XP_011534290.1:p.Gln280Glu
NM_001346813.1:c.3697C>G	NP_001333742.1:p.Gln1233Glu
NM_001363725.1:c.1447C>G	NP_001350654.1:p.Gln483Glu
XM_011535984.2:c.3907C>G	XP_011534286.2:p.Gln1303Glu
XM_011535988.3:c.838C>G	XP_011534290.1:p.Gln280Glu
XM_017011103.2:c.3808C>G	XP_016866592.1:p.Gln1270Glu
XM_017011104.1:c.3778C>G	XP_016866593.1:p.Gln1260Glu
XM_017011105.2:c.3748C>G	XP_016866594.1:p.Gln1250Glu
XM_017011106.2:c.3619C>G	XP_016866595.1:p.Gln1207Glu
XM_017011107.2:c.3598C>G	XP_016866596.1:p.Gln1200Glu
XR_002956289.1:n.3990C>G
NM_001363725.2:c.1447C>G	NP_001350654.1:p.Gln483Glu
NM_001371656.1:c.3826C>G	NP_001358585.1:p.Gln1276Glu
NM_001374820.1:c.3826C>G	NP_001361749.1:p.Gln1276Glu
NM_001374828.1:c.3946C>G MANE Select	NP_001361757.1:p.Gln1316Glu
NM_017519.3:c.3787C>G	NP_059989.3:p.Gln1263Glu