Canonical Allele Identifier: CA366228437

Gene: ARID1B

Linked Data

• dbSNP Id: rs1285024781
• MyVariant Identifiers: chr6:g.157502294G>C (hg19) ; chr6:g.157181160G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181160G>C , CM000668.2:g.157181160G>C	GRCh38
NC_000006.11:g.157502294G>C , CM000668.1:g.157502294G>C	GRCh37
NC_000006.10:g.157543986G>C	NCBI36
NG_032093.1:g.408231G>C
NG_032093.2:g.408231G>C
NG_066624.1:g.410135G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3537G>C	ENSP00000055163.8:p.Glu1179Asp
ENST00000414678.8:c.3606G>C	ENSP00000412835.3:p.Glu1202Asp
ENST00000637015.2:c.3825G>C	ENSP00000489729.2:p.Glu1275Asp
ENST00000319584.11:c.1710G>C	ENSP00000313006.7:p.Glu570Asp
ENST00000346085.10:c.3576G>C	ENSP00000344546.5:p.Glu1192Asp
ENST00000350026.10:c.3288G>C	ENSP00000055163.7:p.Glu1096Asp
ENST00000414678.7:c.1854G>C	ENSP00000412835.2:p.Glu618Asp
ENST00000635849.1:c.1017G>C	ENSP00000490948.1:p.Glu339Asp
ENST00000635957.1:c.651G>C	ENSP00000490385.1:p.Glu217Asp
ENST00000636930.2:c.3696G>C MANE Select	ENSP00000490491.2:p.Glu1232Asp
ENST00000636940.1:n.1693G>C
ENST00000637015.1:c.1064G>C
ENST00000637568.1:c.978G>C
ENST00000637741.1:n.362G>C
ENST00000637810.1:c.1038G>C	ENSP00000489636.1:p.Glu346Asp
ENST00000637904.1:c.1197G>C	ENSP00000490550.1:p.Glu399Asp
ENST00000647938.1:c.3327G>C	ENSP00000498155.1:p.Glu1109Asp
ENST00000319584.10:c.1713G>C	ENSP00000313006.6:p.Glu571Asp
ENST00000346085.9:c.3327G>C	ENSP00000344546.4:p.Glu1109Asp
ENST00000350026.9:c.3288G>C	ENSP00000055163.7:p.Glu1096Asp
ENST00000400790.3:c.489G>C	ENSP00000383596.3:p.Glu163Asp
ENST00000414678.6:c.1854G>C	ENSP00000412835.2:p.Glu618Asp
ENST00000478761.3:c.898G>C
NM_017519.2:c.3288G>C	NP_059989.2:p.Glu1096Asp
NM_020732.3:c.3327G>C	NP_065783.3:p.Glu1109Asp
XM_005267069.3:c.3447G>C	XP_005267126.2:p.Glu1149Asp
XM_011535984.1:c.2526G>C	XP_011534286.1:p.Glu842Asp
XM_011535985.1:c.2346G>C	XP_011534287.1:p.Glu782Asp
XM_011535986.1:c.2106G>C	XP_011534288.1:p.Glu702Asp
XM_011535987.1:c.1725G>C	XP_011534289.1:p.Glu575Asp
XM_011535988.1:c.588G>C	XP_011534290.1:p.Glu196Asp
NM_001346813.1:c.3447G>C	NP_001333742.1:p.Glu1149Asp
NM_001363725.1:c.1197G>C	NP_001350654.1:p.Glu399Asp
XM_011535984.2:c.3657G>C	XP_011534286.2:p.Glu1219Asp
XM_011535988.3:c.588G>C	XP_011534290.1:p.Glu196Asp
XM_017011103.2:c.3558G>C	XP_016866592.1:p.Glu1186Asp
XM_017011104.1:c.3528G>C	XP_016866593.1:p.Glu1176Asp
XM_017011105.2:c.3498G>C	XP_016866594.1:p.Glu1166Asp
XM_017011106.2:c.3369G>C	XP_016866595.1:p.Glu1123Asp
XM_017011107.2:c.3348G>C	XP_016866596.1:p.Glu1116Asp
XR_002956289.1:n.3740G>C
NM_001363725.2:c.1197G>C	NP_001350654.1:p.Glu399Asp
NM_001371656.1:c.3576G>C	NP_001358585.1:p.Glu1192Asp
NM_001374820.1:c.3576G>C	NP_001361749.1:p.Glu1192Asp
NM_001374828.1:c.3696G>C MANE Select	NP_001361757.1:p.Glu1232Asp
NM_017519.3:c.3537G>C	NP_059989.3:p.Glu1179Asp