Canonical Allele Identifier: CA366380974

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157222649A>G (hg19) ; chr6:g.156901515A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901515A>G , CM000668.2:g.156901515A>G	GRCh38
NC_000006.11:g.157222649A>G , CM000668.1:g.157222649A>G	GRCh37
NC_000006.10:g.157264341A>G	NCBI36
NG_032093.1:g.128586A>G
NG_032093.2:g.128586A>G
NG_066624.1:g.130490A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2126A>G	ENSP00000055163.8:p.Gln709Arg
ENST00000414678.8:c.2126A>G	ENSP00000412835.3:p.Gln709Arg
ENST00000637015.2:c.2126A>G	ENSP00000489729.2:p.Gln709Arg
ENST00000319584.11:c.140A>G	ENSP00000313006.7:p.Gln47Arg
ENST00000346085.10:c.2165A>G	ENSP00000344546.5:p.Gln722Arg
ENST00000350026.10:c.1877A>G	ENSP00000055163.7:p.Gln626Arg
ENST00000414678.7:c.374A>G	ENSP00000412835.2:p.Gln125Arg
ENST00000636205.1:n.189A>G
ENST00000636748.1:c.407A>G	ENSP00000489917.1:p.Gln136Arg
ENST00000636930.2:c.2126A>G MANE Select	ENSP00000490491.2:p.Gln709Arg
ENST00000637532.1:c.152A>G	ENSP00000490420.1:p.Gln51Arg
ENST00000638000.1:c.343A>G
ENST00000647938.1:c.1916A>G	ENSP00000498155.1:p.Gln639Arg
ENST00000674190.1:n.833A>G
ENST00000674298.1:c.1866A>G
ENST00000319584.10:c.143A>G	ENSP00000313006.6:p.Gln48Arg
ENST00000346085.9:c.1916A>G	ENSP00000344546.4:p.Gln639Arg
ENST00000350026.9:c.1877A>G	ENSP00000055163.7:p.Gln626Arg
ENST00000414678.6:c.374A>G	ENSP00000412835.2:p.Gln125Arg
NM_017519.2:c.1877A>G	NP_059989.2:p.Gln626Arg
NM_020732.3:c.1916A>G	NP_065783.3:p.Gln639Arg
XM_005267069.3:c.1877A>G	XP_005267126.2:p.Gln626Arg
XM_011535984.1:c.785A>G	XP_011534286.1:p.Gln262Arg
XM_011535985.1:c.785A>G	XP_011534287.1:p.Gln262Arg
XM_011535986.1:c.365A>G	XP_011534288.1:p.Gln122Arg
NM_001346813.1:c.1877A>G	NP_001333742.1:p.Gln626Arg
XM_011535984.2:c.1916A>G	XP_011534286.2:p.Gln639Arg
XM_017011103.2:c.1916A>G	XP_016866592.1:p.Gln639Arg
XM_017011104.1:c.1916A>G	XP_016866593.1:p.Gln639Arg
XM_017011105.2:c.1916A>G	XP_016866594.1:p.Gln639Arg
XM_017011106.2:c.1916A>G	XP_016866595.1:p.Gln639Arg
XM_017011107.2:c.1916A>G	XP_016866596.1:p.Gln639Arg
XR_002956289.1:n.1999A>G
NM_001371656.1:c.2165A>G	NP_001358585.1:p.Gln722Arg
NM_001374820.1:c.2165A>G	NP_001361749.1:p.Gln722Arg
NM_001374828.1:c.2126A>G MANE Select	NP_001361757.1:p.Gln709Arg
NM_017519.3:c.2126A>G	NP_059989.3:p.Gln709Arg