Canonical Allele Identifier: CA366227386

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502165G>C (hg19) ; chr6:g.157181031G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181031G>C , CM000668.2:g.157181031G>C	GRCh38
NC_000006.11:g.157502165G>C , CM000668.1:g.157502165G>C	GRCh37
NC_000006.10:g.157543857G>C	NCBI36
NG_032093.1:g.408102G>C
NG_032093.2:g.408102G>C
NG_066624.1:g.410006G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3408G>C	ENSP00000055163.8:p.Glu1136Asp
ENST00000414678.8:c.3477G>C	ENSP00000412835.3:p.Glu1159Asp
ENST00000637015.2:c.3696G>C	ENSP00000489729.2:p.Glu1232Asp
ENST00000319584.11:c.1581G>C	ENSP00000313006.7:p.Glu527Asp
ENST00000346085.10:c.3447G>C	ENSP00000344546.5:p.Glu1149Asp
ENST00000350026.10:c.3159G>C	ENSP00000055163.7:p.Glu1053Asp
ENST00000414678.7:c.1725G>C	ENSP00000412835.2:p.Glu575Asp
ENST00000635849.1:c.888G>C	ENSP00000490948.1:p.Glu296Asp
ENST00000635957.1:c.522G>C	ENSP00000490385.1:p.Glu174Asp
ENST00000636930.2:c.3567G>C MANE Select	ENSP00000490491.2:p.Glu1189Asp
ENST00000636940.1:n.1564G>C
ENST00000637015.1:c.935G>C
ENST00000637568.1:c.849G>C
ENST00000637741.1:n.233G>C
ENST00000637810.1:c.909G>C	ENSP00000489636.1:p.Glu303Asp
ENST00000637904.1:c.1068G>C	ENSP00000490550.1:p.Glu356Asp
ENST00000647938.1:c.3198G>C	ENSP00000498155.1:p.Glu1066Asp
ENST00000319584.10:c.1584G>C	ENSP00000313006.6:p.Glu528Asp
ENST00000346085.9:c.3198G>C	ENSP00000344546.4:p.Glu1066Asp
ENST00000350026.9:c.3159G>C	ENSP00000055163.7:p.Glu1053Asp
ENST00000400790.3:c.360G>C	ENSP00000383596.3:p.Glu120Asp
ENST00000414678.6:c.1725G>C	ENSP00000412835.2:p.Glu575Asp
ENST00000478761.3:c.769G>C
NM_017519.2:c.3159G>C	NP_059989.2:p.Glu1053Asp
NM_020732.3:c.3198G>C	NP_065783.3:p.Glu1066Asp
XM_005267069.3:c.3318G>C	XP_005267126.2:p.Glu1106Asp
XM_011535984.1:c.2397G>C	XP_011534286.1:p.Glu799Asp
XM_011535985.1:c.2217G>C	XP_011534287.1:p.Glu739Asp
XM_011535986.1:c.1977G>C	XP_011534288.1:p.Glu659Asp
XM_011535987.1:c.1596G>C	XP_011534289.1:p.Glu532Asp
XM_011535988.1:c.459G>C	XP_011534290.1:p.Glu153Asp
NM_001346813.1:c.3318G>C	NP_001333742.1:p.Glu1106Asp
NM_001363725.1:c.1068G>C	NP_001350654.1:p.Glu356Asp
XM_011535984.2:c.3528G>C	XP_011534286.2:p.Glu1176Asp
XM_011535988.3:c.459G>C	XP_011534290.1:p.Glu153Asp
XM_017011103.2:c.3429G>C	XP_016866592.1:p.Glu1143Asp
XM_017011104.1:c.3399G>C	XP_016866593.1:p.Glu1133Asp
XM_017011105.2:c.3369G>C	XP_016866594.1:p.Glu1123Asp
XM_017011106.2:c.3240G>C	XP_016866595.1:p.Glu1080Asp
XM_017011107.2:c.3219G>C	XP_016866596.1:p.Glu1073Asp
XR_002956289.1:n.3611G>C
NM_001363725.2:c.1068G>C	NP_001350654.1:p.Glu356Asp
NM_001371656.1:c.3447G>C	NP_001358585.1:p.Glu1149Asp
NM_001374820.1:c.3447G>C	NP_001361749.1:p.Glu1149Asp
NM_001374828.1:c.3567G>C MANE Select	NP_001361757.1:p.Glu1189Asp
NM_017519.3:c.3408G>C	NP_059989.3:p.Glu1136Asp