Canonical Allele Identifier: CA366241432

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522137A>C (hg19) ; chr6:g.157201003A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201003A>C , CM000668.2:g.157201003A>C	GRCh38
NC_000006.11:g.157522137A>C , CM000668.1:g.157522137A>C	GRCh37
NC_000006.10:g.157563829A>C	NCBI36
NG_032093.1:g.428074A>C
NG_032093.2:g.428074A>C
NG_066624.1:g.429978A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4619A>C	ENSP00000055163.8:p.Asp1540Ala
ENST00000414678.8:c.4688A>C	ENSP00000412835.3:p.Asp1563Ala
ENST00000637015.2:c.4907A>C	ENSP00000489729.2:p.Asp1636Ala
ENST00000346085.10:c.4658A>C	ENSP00000344546.5:p.Asp1553Ala
ENST00000350026.10:c.4370A>C	ENSP00000055163.7:p.Asp1457Ala
ENST00000414678.7:c.2936A>C	ENSP00000412835.2:p.Asp979Ala
ENST00000635849.1:c.2099A>C	ENSP00000490948.1:p.Asp700Ala
ENST00000635957.1:c.1730A>C	ENSP00000490385.1:p.Asp577Ala
ENST00000636227.1:n.3241A>C
ENST00000636254.1:n.698A>C
ENST00000636930.2:c.4778A>C MANE Select	ENSP00000490491.2:p.Asp1593Ala
ENST00000636940.1:n.2775A>C
ENST00000637015.1:c.2146A>C
ENST00000637568.1:c.2060A>C
ENST00000637741.1:n.1444A>C
ENST00000637810.1:c.2120A>C	ENSP00000489636.1:p.Asp707Ala
ENST00000637904.1:c.2279A>C	ENSP00000490550.1:p.Asp760Ala
ENST00000647938.1:c.4409A>C	ENSP00000498155.1:p.Asp1470Ala
ENST00000346085.9:c.4409A>C	ENSP00000344546.4:p.Asp1470Ala
ENST00000350026.9:c.4370A>C	ENSP00000055163.7:p.Asp1457Ala
ENST00000414678.6:c.2936A>C	ENSP00000412835.2:p.Asp979Ala
NM_017519.2:c.4370A>C	NP_059989.2:p.Asp1457Ala
NM_020732.3:c.4409A>C	NP_065783.3:p.Asp1470Ala
XM_005267069.3:c.4529A>C	XP_005267126.2:p.Asp1510Ala
XM_011535984.1:c.3608A>C	XP_011534286.1:p.Asp1203Ala
XM_011535985.1:c.3428A>C	XP_011534287.1:p.Asp1143Ala
XM_011535986.1:c.3188A>C	XP_011534288.1:p.Asp1063Ala
XM_011535987.1:c.2807A>C	XP_011534289.1:p.Asp936Ala
XM_011535988.1:c.1670A>C	XP_011534290.1:p.Asp557Ala
NM_001346813.1:c.4529A>C	NP_001333742.1:p.Asp1510Ala
NM_001363725.1:c.2279A>C	NP_001350654.1:p.Asp760Ala
XM_011535984.2:c.4739A>C	XP_011534286.2:p.Asp1580Ala
XM_011535988.3:c.1670A>C	XP_011534290.1:p.Asp557Ala
XM_017011103.2:c.4640A>C	XP_016866592.1:p.Asp1547Ala
XM_017011104.1:c.4610A>C	XP_016866593.1:p.Asp1537Ala
XM_017011105.2:c.4580A>C	XP_016866594.1:p.Asp1527Ala
XM_017011106.2:c.4451A>C	XP_016866595.1:p.Asp1484Ala
XM_017011107.2:c.4430A>C	XP_016866596.1:p.Asp1477Ala
XR_002956289.1:n.4725A>C
NM_001363725.2:c.2279A>C	NP_001350654.1:p.Asp760Ala
NM_001371656.1:c.4658A>C	NP_001358585.1:p.Asp1553Ala
NM_001374820.1:c.4658A>C	NP_001361749.1:p.Asp1553Ala
NM_001374828.1:c.4778A>C MANE Select	NP_001361757.1:p.Asp1593Ala
NM_017519.3:c.4619A>C	NP_059989.3:p.Asp1540Ala