Canonical Allele Identifier: CA366247805

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206996T>G , CM000668.2:g.157206996T>G	GRCh38
NC_000006.11:g.157528130T>G , CM000668.1:g.157528130T>G	GRCh37
NC_000006.10:g.157569822T>G	NCBI36
NG_032093.1:g.434067T>G
NG_032093.2:g.434067T>G
NG_066624.1:g.435971T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6065T>G	ENSP00000055163.8:p.Val2022Gly
ENST00000414678.8:c.6134T>G	ENSP00000412835.3:p.Val2045Gly
ENST00000637015.2:c.6353T>G	ENSP00000489729.2:p.Val2118Gly
ENST00000346085.10:c.6104T>G	ENSP00000344546.5:p.Val2035Gly
ENST00000350026.10:c.5816T>G	ENSP00000055163.7:p.Val1939Gly
ENST00000414678.7:c.4382T>G	ENSP00000412835.2:p.Val1461Gly
ENST00000635849.1:c.3545T>G	ENSP00000490948.1:p.Val1182Gly
ENST00000635928.1:c.380T>G	ENSP00000489717.1:p.Val127Gly
ENST00000635957.1:c.3176T>G	ENSP00000490385.1:p.Val1059Gly
ENST00000636227.1:n.4687T>G
ENST00000636254.1:n.2144T>G
ENST00000636930.2:c.6224T>G MANE Select	ENSP00000490491.2:p.Val2075Gly
ENST00000636940.1:n.4221T>G
ENST00000637015.1:c.3592T>G
ENST00000637568.1:c.3506T>G
ENST00000637741.1:n.2890T>G
ENST00000637810.1:c.3566T>G	ENSP00000489636.1:p.Val1189Gly
ENST00000637904.1:c.3725T>G	ENSP00000490550.1:p.Val1242Gly
ENST00000637933.1:n.3339T>G
ENST00000647938.1:c.5855T>G	ENSP00000498155.1:p.Val1952Gly
ENST00000346085.9:c.5855T>G	ENSP00000344546.4:p.Val1952Gly
ENST00000350026.9:c.5816T>G	ENSP00000055163.7:p.Val1939Gly
ENST00000414678.6:c.4382T>G	ENSP00000412835.2:p.Val1461Gly
NM_017519.2:c.5816T>G	NP_059989.2:p.Val1939Gly
NM_020732.3:c.5855T>G	NP_065783.3:p.Val1952Gly
XM_005267069.3:c.5975T>G	XP_005267126.2:p.Val1992Gly
XM_011535984.1:c.5054T>G	XP_011534286.1:p.Val1685Gly
XM_011535985.1:c.4874T>G	XP_011534287.1:p.Val1625Gly
XM_011535986.1:c.4634T>G	XP_011534288.1:p.Val1545Gly
XM_011535987.1:c.4253T>G	XP_011534289.1:p.Val1418Gly
XM_011535988.1:c.3116T>G	XP_011534290.1:p.Val1039Gly
NM_001346813.1:c.5975T>G	NP_001333742.1:p.Val1992Gly
NM_001363725.1:c.3725T>G	NP_001350654.1:p.Val1242Gly
XM_011535984.2:c.6185T>G	XP_011534286.2:p.Val2062Gly
XM_011535988.3:c.3116T>G	XP_011534290.1:p.Val1039Gly
XM_017011103.2:c.6086T>G	XP_016866592.1:p.Val2029Gly
XM_017011104.1:c.6056T>G	XP_016866593.1:p.Val2019Gly
XM_017011105.2:c.6026T>G	XP_016866594.1:p.Val2009Gly
XM_017011106.2:c.5897T>G	XP_016866595.1:p.Val1966Gly
XM_017011107.2:c.5876T>G	XP_016866596.1:p.Val1959Gly
XR_002956289.1:n.6171T>G
NM_001363725.2:c.3725T>G	NP_001350654.1:p.Val1242Gly
NM_001371656.1:c.6104T>G	NP_001358585.1:p.Val2035Gly
NM_001374820.1:c.6104T>G	NP_001361749.1:p.Val2035Gly
NM_001374828.1:c.6224T>G MANE Select	NP_001361757.1:p.Val2075Gly
NM_017519.3:c.6065T>G	NP_059989.3:p.Val2022Gly