Canonical Allele Identifier: CA366235027

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511214T>G (hg19) ; chr6:g.157190080T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190080T>G , CM000668.2:g.157190080T>G	GRCh38
NC_000006.11:g.157511214T>G , CM000668.1:g.157511214T>G	GRCh37
NC_000006.10:g.157552906T>G	NCBI36
NG_032093.1:g.417151T>G
NG_032093.2:g.417151T>G
NG_066624.1:g.419055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3942T>G	ENSP00000055163.8:p.Ser1314Arg
ENST00000414678.8:c.4011T>G	ENSP00000412835.3:p.Ser1337Arg
ENST00000637015.2:c.4230T>G	ENSP00000489729.2:p.Ser1410Arg
ENST00000346085.10:c.3981T>G	ENSP00000344546.5:p.Ser1327Arg
ENST00000350026.10:c.3693T>G	ENSP00000055163.7:p.Ser1231Arg
ENST00000414678.7:c.2259T>G	ENSP00000412835.2:p.Ser753Arg
ENST00000635849.1:c.1422T>G	ENSP00000490948.1:p.Ser474Arg
ENST00000635957.1:c.1053T>G	ENSP00000490385.1:p.Ser351Arg
ENST00000636930.2:c.4101T>G MANE Select	ENSP00000490491.2:p.Ser1367Arg
ENST00000636940.1:n.2098T>G
ENST00000637015.1:c.1469T>G
ENST00000637568.1:c.1383T>G
ENST00000637741.1:n.767T>G
ENST00000637810.1:c.1443T>G	ENSP00000489636.1:p.Ser481Arg
ENST00000637904.1:c.1602T>G	ENSP00000490550.1:p.Ser534Arg
ENST00000647938.1:c.3732T>G	ENSP00000498155.1:p.Ser1244Arg
ENST00000346085.9:c.3732T>G	ENSP00000344546.4:p.Ser1244Arg
ENST00000350026.9:c.3693T>G	ENSP00000055163.7:p.Ser1231Arg
ENST00000414678.6:c.2259T>G	ENSP00000412835.2:p.Ser753Arg
NM_017519.2:c.3693T>G	NP_059989.2:p.Ser1231Arg
NM_020732.3:c.3732T>G	NP_065783.3:p.Ser1244Arg
XM_005267069.3:c.3852T>G	XP_005267126.2:p.Ser1284Arg
XM_011535984.1:c.2931T>G	XP_011534286.1:p.Ser977Arg
XM_011535985.1:c.2751T>G	XP_011534287.1:p.Ser917Arg
XM_011535986.1:c.2511T>G	XP_011534288.1:p.Ser837Arg
XM_011535987.1:c.2130T>G	XP_011534289.1:p.Ser710Arg
XM_011535988.1:c.993T>G	XP_011534290.1:p.Ser331Arg
NM_001346813.1:c.3852T>G	NP_001333742.1:p.Ser1284Arg
NM_001363725.1:c.1602T>G	NP_001350654.1:p.Ser534Arg
XM_011535984.2:c.4062T>G	XP_011534286.2:p.Ser1354Arg
XM_011535988.3:c.993T>G	XP_011534290.1:p.Ser331Arg
XM_017011103.2:c.3963T>G	XP_016866592.1:p.Ser1321Arg
XM_017011104.1:c.3933T>G	XP_016866593.1:p.Ser1311Arg
XM_017011105.2:c.3903T>G	XP_016866594.1:p.Ser1301Arg
XM_017011106.2:c.3774T>G	XP_016866595.1:p.Ser1258Arg
XM_017011107.2:c.3753T>G	XP_016866596.1:p.Ser1251Arg
XR_002956289.1:n.4145T>G
NM_001363725.2:c.1602T>G	NP_001350654.1:p.Ser534Arg
NM_001371656.1:c.3981T>G	NP_001358585.1:p.Ser1327Arg
NM_001374820.1:c.3981T>G	NP_001361749.1:p.Ser1327Arg
NM_001374828.1:c.4101T>G MANE Select	NP_001361757.1:p.Ser1367Arg
NM_017519.3:c.3942T>G	NP_059989.3:p.Ser1314Arg