Canonical Allele Identifier: CA366242106

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522280C>G (hg19) ; chr6:g.157201146C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201146C>G , CM000668.2:g.157201146C>G	GRCh38
NC_000006.11:g.157522280C>G , CM000668.1:g.157522280C>G	GRCh37
NC_000006.10:g.157563972C>G	NCBI36
NG_032093.1:g.428217C>G
NG_032093.2:g.428217C>G
NG_066624.1:g.430121C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4762C>G	ENSP00000055163.8:p.Gln1588Glu
ENST00000414678.8:c.4831C>G	ENSP00000412835.3:p.Gln1611Glu
ENST00000637015.2:c.5050C>G	ENSP00000489729.2:p.Gln1684Glu
ENST00000346085.10:c.4801C>G	ENSP00000344546.5:p.Gln1601Glu
ENST00000350026.10:c.4513C>G	ENSP00000055163.7:p.Gln1505Glu
ENST00000414678.7:c.3079C>G	ENSP00000412835.2:p.Gln1027Glu
ENST00000635849.1:c.2242C>G	ENSP00000490948.1:p.Gln748Glu
ENST00000635957.1:c.1873C>G	ENSP00000490385.1:p.Gln625Glu
ENST00000636227.1:n.3384C>G
ENST00000636254.1:n.841C>G
ENST00000636930.2:c.4921C>G MANE Select	ENSP00000490491.2:p.Gln1641Glu
ENST00000636940.1:n.2918C>G
ENST00000637015.1:c.2289C>G
ENST00000637568.1:c.2203C>G
ENST00000637741.1:n.1587C>G
ENST00000637810.1:c.2263C>G	ENSP00000489636.1:p.Gln755Glu
ENST00000637904.1:c.2422C>G	ENSP00000490550.1:p.Gln808Glu
ENST00000647938.1:c.4552C>G	ENSP00000498155.1:p.Gln1518Glu
ENST00000346085.9:c.4552C>G	ENSP00000344546.4:p.Gln1518Glu
ENST00000350026.9:c.4513C>G	ENSP00000055163.7:p.Gln1505Glu
ENST00000414678.6:c.3079C>G	ENSP00000412835.2:p.Gln1027Glu
NM_017519.2:c.4513C>G	NP_059989.2:p.Gln1505Glu
NM_020732.3:c.4552C>G	NP_065783.3:p.Gln1518Glu
XM_005267069.3:c.4672C>G	XP_005267126.2:p.Gln1558Glu
XM_011535984.1:c.3751C>G	XP_011534286.1:p.Gln1251Glu
XM_011535985.1:c.3571C>G	XP_011534287.1:p.Gln1191Glu
XM_011535986.1:c.3331C>G	XP_011534288.1:p.Gln1111Glu
XM_011535987.1:c.2950C>G	XP_011534289.1:p.Gln984Glu
XM_011535988.1:c.1813C>G	XP_011534290.1:p.Gln605Glu
NM_001346813.1:c.4672C>G	NP_001333742.1:p.Gln1558Glu
NM_001363725.1:c.2422C>G	NP_001350654.1:p.Gln808Glu
XM_011535984.2:c.4882C>G	XP_011534286.2:p.Gln1628Glu
XM_011535988.3:c.1813C>G	XP_011534290.1:p.Gln605Glu
XM_017011103.2:c.4783C>G	XP_016866592.1:p.Gln1595Glu
XM_017011104.1:c.4753C>G	XP_016866593.1:p.Gln1585Glu
XM_017011105.2:c.4723C>G	XP_016866594.1:p.Gln1575Glu
XM_017011106.2:c.4594C>G	XP_016866595.1:p.Gln1532Glu
XM_017011107.2:c.4573C>G	XP_016866596.1:p.Gln1525Glu
XR_002956289.1:n.4868C>G
NM_001363725.2:c.2422C>G	NP_001350654.1:p.Gln808Glu
NM_001371656.1:c.4801C>G	NP_001358585.1:p.Gln1601Glu
NM_001374820.1:c.4801C>G	NP_001361749.1:p.Gln1601Glu
NM_001374828.1:c.4921C>G MANE Select	NP_001361757.1:p.Gln1641Glu
NM_017519.3:c.4762C>G	NP_059989.3:p.Gln1588Glu