Canonical Allele Identifier: CA366242510

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522452T>G (hg19) ; chr6:g.157201318T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201318T>G , CM000668.2:g.157201318T>G	GRCh38
NC_000006.11:g.157522452T>G , CM000668.1:g.157522452T>G	GRCh37
NC_000006.10:g.157564144T>G	NCBI36
NG_032093.1:g.428389T>G
NG_032093.2:g.428389T>G
NG_066624.1:g.430293T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4934T>G	ENSP00000055163.8:p.Leu1645Arg
ENST00000414678.8:c.5003T>G	ENSP00000412835.3:p.Leu1668Arg
ENST00000637015.2:c.5222T>G	ENSP00000489729.2:p.Leu1741Arg
ENST00000346085.10:c.4973T>G	ENSP00000344546.5:p.Leu1658Arg
ENST00000350026.10:c.4685T>G	ENSP00000055163.7:p.Leu1562Arg
ENST00000414678.7:c.3251T>G	ENSP00000412835.2:p.Leu1084Arg
ENST00000635849.1:c.2414T>G	ENSP00000490948.1:p.Leu805Arg
ENST00000635957.1:c.2045T>G	ENSP00000490385.1:p.Leu682Arg
ENST00000636227.1:n.3556T>G
ENST00000636254.1:n.1013T>G
ENST00000636930.2:c.5093T>G MANE Select	ENSP00000490491.2:p.Leu1698Arg
ENST00000636940.1:n.3090T>G
ENST00000637015.1:c.2461T>G
ENST00000637568.1:c.2375T>G
ENST00000637741.1:n.1759T>G
ENST00000637810.1:c.2435T>G	ENSP00000489636.1:p.Leu812Arg
ENST00000637904.1:c.2594T>G	ENSP00000490550.1:p.Leu865Arg
ENST00000647938.1:c.4724T>G	ENSP00000498155.1:p.Leu1575Arg
ENST00000346085.9:c.4724T>G	ENSP00000344546.4:p.Leu1575Arg
ENST00000350026.9:c.4685T>G	ENSP00000055163.7:p.Leu1562Arg
ENST00000414678.6:c.3251T>G	ENSP00000412835.2:p.Leu1084Arg
NM_017519.2:c.4685T>G	NP_059989.2:p.Leu1562Arg
NM_020732.3:c.4724T>G	NP_065783.3:p.Leu1575Arg
XM_005267069.3:c.4844T>G	XP_005267126.2:p.Leu1615Arg
XM_011535984.1:c.3923T>G	XP_011534286.1:p.Leu1308Arg
XM_011535985.1:c.3743T>G	XP_011534287.1:p.Leu1248Arg
XM_011535986.1:c.3503T>G	XP_011534288.1:p.Leu1168Arg
XM_011535987.1:c.3122T>G	XP_011534289.1:p.Leu1041Arg
XM_011535988.1:c.1985T>G	XP_011534290.1:p.Leu662Arg
NM_001346813.1:c.4844T>G	NP_001333742.1:p.Leu1615Arg
NM_001363725.1:c.2594T>G	NP_001350654.1:p.Leu865Arg
XM_011535984.2:c.5054T>G	XP_011534286.2:p.Leu1685Arg
XM_011535988.3:c.1985T>G	XP_011534290.1:p.Leu662Arg
XM_017011103.2:c.4955T>G	XP_016866592.1:p.Leu1652Arg
XM_017011104.1:c.4925T>G	XP_016866593.1:p.Leu1642Arg
XM_017011105.2:c.4895T>G	XP_016866594.1:p.Leu1632Arg
XM_017011106.2:c.4766T>G	XP_016866595.1:p.Leu1589Arg
XM_017011107.2:c.4745T>G	XP_016866596.1:p.Leu1582Arg
XR_002956289.1:n.5040T>G
NM_001363725.2:c.2594T>G	NP_001350654.1:p.Leu865Arg
NM_001371656.1:c.4973T>G	NP_001358585.1:p.Leu1658Arg
NM_001374820.1:c.4973T>G	NP_001361749.1:p.Leu1658Arg
NM_001374828.1:c.5093T>G MANE Select	NP_001361757.1:p.Leu1698Arg
NM_017519.3:c.4934T>G	NP_059989.3:p.Leu1645Arg