Canonical Allele Identifier: CA366389131

Gene: ARID1B

Linked Data

• dbSNP Id: rs1318124895
• gnomAD v2: 6-157470001-G-A
• MyVariant Identifiers: chr6:g.157470001G>A (hg19) ; chr6:g.157148867G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148867G>A , CM000668.2:g.157148867G>A	GRCh38
NC_000006.11:g.157470001G>A , CM000668.1:g.157470001G>A	GRCh37
NC_000006.10:g.157511693G>A	NCBI36
NG_032093.1:g.375938G>A
NG_032093.2:g.375938G>A
NG_066624.1:g.377842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3005G>A	ENSP00000055163.8:p.Gly1002Glu
ENST00000414678.8:c.2915G>A	ENSP00000412835.3:p.Gly972Glu
ENST00000637015.2:c.3005G>A	ENSP00000489729.2:p.Gly1002Glu
ENST00000319584.11:c.1019G>A	ENSP00000313006.7:p.Gly340Glu
ENST00000346085.10:c.3044G>A	ENSP00000344546.5:p.Gly1015Glu
ENST00000350026.10:c.2756G>A	ENSP00000055163.7:p.Gly919Glu
ENST00000414678.7:c.1163G>A	ENSP00000412835.2:p.Gly388Glu
ENST00000452544.2:n.906G>A
ENST00000635849.1:c.326G>A	ENSP00000490948.1:p.Gly109Glu
ENST00000636426.1:n.139G>A
ENST00000636930.2:c.3005G>A MANE Select	ENSP00000490491.2:p.Gly1002Glu
ENST00000637015.1:c.244G>A
ENST00000637568.1:c.48G>A
ENST00000637810.1:c.506G>A	ENSP00000489636.1:p.Gly169Glu
ENST00000637904.1:c.506G>A	ENSP00000490550.1:p.Gly169Glu
ENST00000647938.1:c.2795G>A	ENSP00000498155.1:p.Gly932Glu
ENST00000674190.1:n.1754G>A
ENST00000319584.10:c.1022G>A	ENSP00000313006.6:p.Gly341Glu
ENST00000346085.9:c.2795G>A	ENSP00000344546.4:p.Gly932Glu
ENST00000350026.9:c.2756G>A	ENSP00000055163.7:p.Gly919Glu
ENST00000414678.6:c.1163G>A	ENSP00000412835.2:p.Gly388Glu
ENST00000452544.1:n.852G>A
ENST00000478761.3:c.78G>A
NM_017519.2:c.2756G>A	NP_059989.2:p.Gly919Glu
NM_020732.3:c.2795G>A	NP_065783.3:p.Gly932Glu
XM_005267069.3:c.2756G>A	XP_005267126.2:p.Gly919Glu
XM_011535984.1:c.1706G>A	XP_011534286.1:p.Gly569Glu
XM_011535985.1:c.1526G>A	XP_011534287.1:p.Gly509Glu
XM_011535986.1:c.1286G>A	XP_011534288.1:p.Gly429Glu
XM_011535987.1:c.905G>A	XP_011534289.1:p.Gly302Glu
XM_011535988.1:c.-20+15660G>A	XP_011534290.1:n.-20+15660G>A
NM_001346813.1:c.2756G>A	NP_001333742.1:p.Gly919Glu
NM_001363725.1:c.506G>A	NP_001350654.1:p.Gly169Glu
XM_011535984.2:c.2837G>A	XP_011534286.2:p.Gly946Glu
XM_011535988.3:c.-20+15660G>A	XP_011534290.1:n.-20+15660G>A
XM_017011103.2:c.2837G>A	XP_016866592.1:p.Gly946Glu
XM_017011104.1:c.2837G>A	XP_016866593.1:p.Gly946Glu
XM_017011105.2:c.2837G>A	XP_016866594.1:p.Gly946Glu
XM_017011106.2:c.2837G>A	XP_016866595.1:p.Gly946Glu
XM_017011107.2:c.2657G>A	XP_016866596.1:p.Gly886Glu
XR_002956289.1:n.2920G>A
NM_001363725.2:c.506G>A	NP_001350654.1:p.Gly169Glu
NM_001371656.1:c.3044G>A	NP_001358585.1:p.Gly1015Glu
NM_001374820.1:c.3044G>A	NP_001361749.1:p.Gly1015Glu
NM_001374828.1:c.3005G>A MANE Select	NP_001361757.1:p.Gly1002Glu
NM_017519.3:c.3005G>A	NP_059989.3:p.Gly1002Glu