Canonical Allele Identifier: CA366246188

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157527521A>G (hg19) ; chr6:g.157206387A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206387A>G , CM000668.2:g.157206387A>G	GRCh38
NC_000006.11:g.157527521A>G , CM000668.1:g.157527521A>G	GRCh37
NC_000006.10:g.157569213A>G	NCBI36
NG_032093.1:g.433458A>G
NG_032093.2:g.433458A>G
NG_066624.1:g.435362A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5456A>G	ENSP00000055163.8:p.Glu1819Gly
ENST00000414678.8:c.5525A>G	ENSP00000412835.3:p.Glu1842Gly
ENST00000637015.2:c.5744A>G	ENSP00000489729.2:p.Glu1915Gly
ENST00000346085.10:c.5495A>G	ENSP00000344546.5:p.Glu1832Gly
ENST00000350026.10:c.5207A>G	ENSP00000055163.7:p.Glu1736Gly
ENST00000414678.7:c.3773A>G	ENSP00000412835.2:p.Glu1258Gly
ENST00000635849.1:c.2936A>G	ENSP00000490948.1:p.Glu979Gly
ENST00000635957.1:c.2567A>G	ENSP00000490385.1:p.Glu856Gly
ENST00000636227.1:n.4078A>G
ENST00000636254.1:n.1535A>G
ENST00000636930.2:c.5615A>G MANE Select	ENSP00000490491.2:p.Glu1872Gly
ENST00000636940.1:n.3612A>G
ENST00000637015.1:c.2983A>G
ENST00000637568.1:c.2897A>G
ENST00000637741.1:n.2281A>G
ENST00000637810.1:c.2957A>G	ENSP00000489636.1:p.Glu986Gly
ENST00000637904.1:c.3116A>G	ENSP00000490550.1:p.Glu1039Gly
ENST00000637933.1:n.2730A>G
ENST00000647938.1:c.5246A>G	ENSP00000498155.1:p.Glu1749Gly
ENST00000346085.9:c.5246A>G	ENSP00000344546.4:p.Glu1749Gly
ENST00000350026.9:c.5207A>G	ENSP00000055163.7:p.Glu1736Gly
ENST00000414678.6:c.3773A>G	ENSP00000412835.2:p.Glu1258Gly
NM_017519.2:c.5207A>G	NP_059989.2:p.Glu1736Gly
NM_020732.3:c.5246A>G	NP_065783.3:p.Glu1749Gly
XM_005267069.3:c.5366A>G	XP_005267126.2:p.Glu1789Gly
XM_011535984.1:c.4445A>G	XP_011534286.1:p.Glu1482Gly
XM_011535985.1:c.4265A>G	XP_011534287.1:p.Glu1422Gly
XM_011535986.1:c.4025A>G	XP_011534288.1:p.Glu1342Gly
XM_011535987.1:c.3644A>G	XP_011534289.1:p.Glu1215Gly
XM_011535988.1:c.2507A>G	XP_011534290.1:p.Glu836Gly
NM_001346813.1:c.5366A>G	NP_001333742.1:p.Glu1789Gly
NM_001363725.1:c.3116A>G	NP_001350654.1:p.Glu1039Gly
XM_011535984.2:c.5576A>G	XP_011534286.2:p.Glu1859Gly
XM_011535988.3:c.2507A>G	XP_011534290.1:p.Glu836Gly
XM_017011103.2:c.5477A>G	XP_016866592.1:p.Glu1826Gly
XM_017011104.1:c.5447A>G	XP_016866593.1:p.Glu1816Gly
XM_017011105.2:c.5417A>G	XP_016866594.1:p.Glu1806Gly
XM_017011106.2:c.5288A>G	XP_016866595.1:p.Glu1763Gly
XM_017011107.2:c.5267A>G	XP_016866596.1:p.Glu1756Gly
XR_002956289.1:n.5562A>G
NM_001363725.2:c.3116A>G	NP_001350654.1:p.Glu1039Gly
NM_001371656.1:c.5495A>G	NP_001358585.1:p.Glu1832Gly
NM_001374820.1:c.5495A>G	NP_001361749.1:p.Glu1832Gly
NM_001374828.1:c.5615A>G MANE Select	NP_001361757.1:p.Glu1872Gly
NM_017519.3:c.5456A>G	NP_059989.3:p.Glu1819Gly