Canonical Allele Identifier: CA366242232

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522337C>G (hg19) ; chr6:g.157201203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201203C>G , CM000668.2:g.157201203C>G	GRCh38
NC_000006.11:g.157522337C>G , CM000668.1:g.157522337C>G	GRCh37
NC_000006.10:g.157564029C>G	NCBI36
NG_032093.1:g.428274C>G
NG_032093.2:g.428274C>G
NG_066624.1:g.430178C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4819C>G	ENSP00000055163.8:p.Gln1607Glu
ENST00000414678.8:c.4888C>G	ENSP00000412835.3:p.Gln1630Glu
ENST00000637015.2:c.5107C>G	ENSP00000489729.2:p.Gln1703Glu
ENST00000346085.10:c.4858C>G	ENSP00000344546.5:p.Gln1620Glu
ENST00000350026.10:c.4570C>G	ENSP00000055163.7:p.Gln1524Glu
ENST00000414678.7:c.3136C>G	ENSP00000412835.2:p.Gln1046Glu
ENST00000635849.1:c.2299C>G	ENSP00000490948.1:p.Gln767Glu
ENST00000635957.1:c.1930C>G	ENSP00000490385.1:p.Gln644Glu
ENST00000636227.1:n.3441C>G
ENST00000636254.1:n.898C>G
ENST00000636930.2:c.4978C>G MANE Select	ENSP00000490491.2:p.Gln1660Glu
ENST00000636940.1:n.2975C>G
ENST00000637015.1:c.2346C>G
ENST00000637568.1:c.2260C>G
ENST00000637741.1:n.1644C>G
ENST00000637810.1:c.2320C>G	ENSP00000489636.1:p.Gln774Glu
ENST00000637904.1:c.2479C>G	ENSP00000490550.1:p.Gln827Glu
ENST00000647938.1:c.4609C>G	ENSP00000498155.1:p.Gln1537Glu
ENST00000346085.9:c.4609C>G	ENSP00000344546.4:p.Gln1537Glu
ENST00000350026.9:c.4570C>G	ENSP00000055163.7:p.Gln1524Glu
ENST00000414678.6:c.3136C>G	ENSP00000412835.2:p.Gln1046Glu
NM_017519.2:c.4570C>G	NP_059989.2:p.Gln1524Glu
NM_020732.3:c.4609C>G	NP_065783.3:p.Gln1537Glu
XM_005267069.3:c.4729C>G	XP_005267126.2:p.Gln1577Glu
XM_011535984.1:c.3808C>G	XP_011534286.1:p.Gln1270Glu
XM_011535985.1:c.3628C>G	XP_011534287.1:p.Gln1210Glu
XM_011535986.1:c.3388C>G	XP_011534288.1:p.Gln1130Glu
XM_011535987.1:c.3007C>G	XP_011534289.1:p.Gln1003Glu
XM_011535988.1:c.1870C>G	XP_011534290.1:p.Gln624Glu
NM_001346813.1:c.4729C>G	NP_001333742.1:p.Gln1577Glu
NM_001363725.1:c.2479C>G	NP_001350654.1:p.Gln827Glu
XM_011535984.2:c.4939C>G	XP_011534286.2:p.Gln1647Glu
XM_011535988.3:c.1870C>G	XP_011534290.1:p.Gln624Glu
XM_017011103.2:c.4840C>G	XP_016866592.1:p.Gln1614Glu
XM_017011104.1:c.4810C>G	XP_016866593.1:p.Gln1604Glu
XM_017011105.2:c.4780C>G	XP_016866594.1:p.Gln1594Glu
XM_017011106.2:c.4651C>G	XP_016866595.1:p.Gln1551Glu
XM_017011107.2:c.4630C>G	XP_016866596.1:p.Gln1544Glu
XR_002956289.1:n.4925C>G
NM_001363725.2:c.2479C>G	NP_001350654.1:p.Gln827Glu
NM_001371656.1:c.4858C>G	NP_001358585.1:p.Gln1620Glu
NM_001374820.1:c.4858C>G	NP_001361749.1:p.Gln1620Glu
NM_001374828.1:c.4978C>G MANE Select	NP_001361757.1:p.Gln1660Glu
NM_017519.3:c.4819C>G	NP_059989.3:p.Gln1607Glu