Canonical Allele Identifier: CA366235124

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511225T>C (hg19) ; chr6:g.157190091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190091T>C , CM000668.2:g.157190091T>C	GRCh38
NC_000006.11:g.157511225T>C , CM000668.1:g.157511225T>C	GRCh37
NC_000006.10:g.157552917T>C	NCBI36
NG_032093.1:g.417162T>C
NG_032093.2:g.417162T>C
NG_066624.1:g.419066T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3953T>C	ENSP00000055163.8:p.Phe1318Ser
ENST00000414678.8:c.4022T>C	ENSP00000412835.3:p.Phe1341Ser
ENST00000637015.2:c.4241T>C	ENSP00000489729.2:p.Phe1414Ser
ENST00000346085.10:c.3992T>C	ENSP00000344546.5:p.Phe1331Ser
ENST00000350026.10:c.3704T>C	ENSP00000055163.7:p.Phe1235Ser
ENST00000414678.7:c.2270T>C	ENSP00000412835.2:p.Phe757Ser
ENST00000635849.1:c.1433T>C	ENSP00000490948.1:p.Phe478Ser
ENST00000635957.1:c.1064T>C	ENSP00000490385.1:p.Phe355Ser
ENST00000636930.2:c.4112T>C MANE Select	ENSP00000490491.2:p.Phe1371Ser
ENST00000636940.1:n.2109T>C
ENST00000637015.1:c.1480T>C
ENST00000637568.1:c.1394T>C
ENST00000637741.1:n.778T>C
ENST00000637810.1:c.1454T>C	ENSP00000489636.1:p.Phe485Ser
ENST00000637904.1:c.1613T>C	ENSP00000490550.1:p.Phe538Ser
ENST00000647938.1:c.3743T>C	ENSP00000498155.1:p.Phe1248Ser
ENST00000346085.9:c.3743T>C	ENSP00000344546.4:p.Phe1248Ser
ENST00000350026.9:c.3704T>C	ENSP00000055163.7:p.Phe1235Ser
ENST00000414678.6:c.2270T>C	ENSP00000412835.2:p.Phe757Ser
NM_017519.2:c.3704T>C	NP_059989.2:p.Phe1235Ser
NM_020732.3:c.3743T>C	NP_065783.3:p.Phe1248Ser
XM_005267069.3:c.3863T>C	XP_005267126.2:p.Phe1288Ser
XM_011535984.1:c.2942T>C	XP_011534286.1:p.Phe981Ser
XM_011535985.1:c.2762T>C	XP_011534287.1:p.Phe921Ser
XM_011535986.1:c.2522T>C	XP_011534288.1:p.Phe841Ser
XM_011535987.1:c.2141T>C	XP_011534289.1:p.Phe714Ser
XM_011535988.1:c.1004T>C	XP_011534290.1:p.Phe335Ser
NM_001346813.1:c.3863T>C	NP_001333742.1:p.Phe1288Ser
NM_001363725.1:c.1613T>C	NP_001350654.1:p.Phe538Ser
XM_011535984.2:c.4073T>C	XP_011534286.2:p.Phe1358Ser
XM_011535988.3:c.1004T>C	XP_011534290.1:p.Phe335Ser
XM_017011103.2:c.3974T>C	XP_016866592.1:p.Phe1325Ser
XM_017011104.1:c.3944T>C	XP_016866593.1:p.Phe1315Ser
XM_017011105.2:c.3914T>C	XP_016866594.1:p.Phe1305Ser
XM_017011106.2:c.3785T>C	XP_016866595.1:p.Phe1262Ser
XM_017011107.2:c.3764T>C	XP_016866596.1:p.Phe1255Ser
XR_002956289.1:n.4156T>C
NM_001363725.2:c.1613T>C	NP_001350654.1:p.Phe538Ser
NM_001371656.1:c.3992T>C	NP_001358585.1:p.Phe1331Ser
NM_001374820.1:c.3992T>C	NP_001361749.1:p.Phe1331Ser
NM_001374828.1:c.4112T>C MANE Select	NP_001361757.1:p.Phe1371Ser
NM_017519.3:c.3953T>C	NP_059989.3:p.Phe1318Ser