Canonical Allele Identifier: CA366234046

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3787C>A	ENSP00000055163.8:p.Gln1263Lys
ENST00000414678.8:c.3856C>A	ENSP00000412835.3:p.Gln1286Lys
ENST00000637015.2:c.4075C>A	ENSP00000489729.2:p.Gln1359Lys
ENST00000346085.10:c.3826C>A	ENSP00000344546.5:p.Gln1276Lys
ENST00000350026.10:c.3538C>A	ENSP00000055163.7:p.Gln1180Lys
ENST00000414678.7:c.2104C>A	ENSP00000412835.2:p.Gln702Lys
ENST00000635849.1:c.1267C>A	ENSP00000490948.1:p.Gln423Lys
ENST00000635957.1:c.901C>A	ENSP00000490385.1:p.Gln301Lys
ENST00000636930.2:c.3946C>A MANE Select	ENSP00000490491.2:p.Gln1316Lys
ENST00000636940.1:n.1943C>A
ENST00000637015.1:c.1314C>A
ENST00000637568.1:c.1228C>A
ENST00000637741.1:n.612C>A
ENST00000637810.1:c.1288C>A	ENSP00000489636.1:p.Gln430Lys
ENST00000637904.1:c.1447C>A	ENSP00000490550.1:p.Gln483Lys
ENST00000647938.1:c.3577C>A	ENSP00000498155.1:p.Gln1193Lys
ENST00000346085.9:c.3577C>A	ENSP00000344546.4:p.Gln1193Lys
ENST00000350026.9:c.3538C>A	ENSP00000055163.7:p.Gln1180Lys
ENST00000414678.6:c.2104C>A	ENSP00000412835.2:p.Gln702Lys
NM_017519.2:c.3538C>A	NP_059989.2:p.Gln1180Lys
NM_020732.3:c.3577C>A	NP_065783.3:p.Gln1193Lys
XM_005267069.3:c.3697C>A	XP_005267126.2:p.Gln1233Lys
XM_011535984.1:c.2776C>A	XP_011534286.1:p.Gln926Lys
XM_011535985.1:c.2596C>A	XP_011534287.1:p.Gln866Lys
XM_011535986.1:c.2356C>A	XP_011534288.1:p.Gln786Lys
XM_011535987.1:c.1975C>A	XP_011534289.1:p.Gln659Lys
XM_011535988.1:c.838C>A	XP_011534290.1:p.Gln280Lys
NM_001346813.1:c.3697C>A	NP_001333742.1:p.Gln1233Lys
NM_001363725.1:c.1447C>A	NP_001350654.1:p.Gln483Lys
XM_011535984.2:c.3907C>A	XP_011534286.2:p.Gln1303Lys
XM_011535988.3:c.838C>A	XP_011534290.1:p.Gln280Lys
XM_017011103.2:c.3808C>A	XP_016866592.1:p.Gln1270Lys
XM_017011104.1:c.3778C>A	XP_016866593.1:p.Gln1260Lys
XM_017011105.2:c.3748C>A	XP_016866594.1:p.Gln1250Lys
XM_017011106.2:c.3619C>A	XP_016866595.1:p.Gln1207Lys
XM_017011107.2:c.3598C>A	XP_016866596.1:p.Gln1200Lys
XR_002956289.1:n.3990C>A
NM_001363725.2:c.1447C>A	NP_001350654.1:p.Gln483Lys
NM_001371656.1:c.3826C>A	NP_001358585.1:p.Gln1276Lys
NM_001374820.1:c.3826C>A	NP_001361749.1:p.Gln1276Lys
NM_001374828.1:c.3946C>A MANE Select	NP_001361757.1:p.Gln1316Lys
NM_017519.3:c.3787C>A	NP_059989.3:p.Gln1263Lys