Canonical Allele Identifier: CA4067768

Gene: ARID1B

Linked Data

• dbSNP Id: rs770072973
• ExAC: 6:157522524 C / A
• gnomAD v2: 6-157522524-C-A
• gnomAD v4: 6-157201390-C-A
• MyVariant Identifiers: chr6:g.157522524C>A (hg19) ; chr6:g.157201390C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201390C>A , CM000668.2:g.157201390C>A	GRCh38
NC_000006.11:g.157522524C>A , CM000668.1:g.157522524C>A	GRCh37
NC_000006.10:g.157564216C>A	NCBI36
NG_032093.1:g.428461C>A
NG_032093.2:g.428461C>A
NG_066624.1:g.430365C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5006C>A	ENSP00000055163.8:p.Pro1669Gln
ENST00000414678.8:c.5075C>A	ENSP00000412835.3:p.Pro1692Gln
ENST00000637015.2:c.5294C>A	ENSP00000489729.2:p.Pro1765Gln
ENST00000346085.10:c.5045C>A	ENSP00000344546.5:p.Pro1682Gln
ENST00000350026.10:c.4757C>A	ENSP00000055163.7:p.Pro1586Gln
ENST00000414678.7:c.3323C>A	ENSP00000412835.2:p.Pro1108Gln
ENST00000635849.1:c.2486C>A	ENSP00000490948.1:p.Pro829Gln
ENST00000635957.1:c.2117C>A	ENSP00000490385.1:p.Pro706Gln
ENST00000636227.1:n.3628C>A
ENST00000636254.1:n.1085C>A
ENST00000636930.2:c.5165C>A MANE Select	ENSP00000490491.2:p.Pro1722Gln
ENST00000636940.1:n.3162C>A
ENST00000637015.1:c.2533C>A
ENST00000637568.1:c.2447C>A
ENST00000637741.1:n.1831C>A
ENST00000637810.1:c.2507C>A	ENSP00000489636.1:p.Pro836Gln
ENST00000637904.1:c.2666C>A	ENSP00000490550.1:p.Pro889Gln
ENST00000647938.1:c.4796C>A	ENSP00000498155.1:p.Pro1599Gln
ENST00000346085.9:c.4796C>A	ENSP00000344546.4:p.Pro1599Gln
ENST00000350026.9:c.4757C>A	ENSP00000055163.7:p.Pro1586Gln
ENST00000414678.6:c.3323C>A	ENSP00000412835.2:p.Pro1108Gln
NM_017519.2:c.4757C>A	NP_059989.2:p.Pro1586Gln
NM_020732.3:c.4796C>A	NP_065783.3:p.Pro1599Gln
XM_005267069.3:c.4916C>A	XP_005267126.2:p.Pro1639Gln
XM_011535984.1:c.3995C>A	XP_011534286.1:p.Pro1332Gln
XM_011535985.1:c.3815C>A	XP_011534287.1:p.Pro1272Gln
XM_011535986.1:c.3575C>A	XP_011534288.1:p.Pro1192Gln
XM_011535987.1:c.3194C>A	XP_011534289.1:p.Pro1065Gln
XM_011535988.1:c.2057C>A	XP_011534290.1:p.Pro686Gln
NM_001346813.1:c.4916C>A	NP_001333742.1:p.Pro1639Gln
NM_001363725.1:c.2666C>A	NP_001350654.1:p.Pro889Gln
XM_011535984.2:c.5126C>A	XP_011534286.2:p.Pro1709Gln
XM_011535988.3:c.2057C>A	XP_011534290.1:p.Pro686Gln
XM_017011103.2:c.5027C>A	XP_016866592.1:p.Pro1676Gln
XM_017011104.1:c.4997C>A	XP_016866593.1:p.Pro1666Gln
XM_017011105.2:c.4967C>A	XP_016866594.1:p.Pro1656Gln
XM_017011106.2:c.4838C>A	XP_016866595.1:p.Pro1613Gln
XM_017011107.2:c.4817C>A	XP_016866596.1:p.Pro1606Gln
XR_002956289.1:n.5112C>A
NM_001363725.2:c.2666C>A	NP_001350654.1:p.Pro889Gln
NM_001371656.1:c.5045C>A	NP_001358585.1:p.Pro1682Gln
NM_001374820.1:c.5045C>A	NP_001361749.1:p.Pro1682Gln
NM_001374828.1:c.5165C>A MANE Select	NP_001361757.1:p.Pro1722Gln
NM_017519.3:c.5006C>A	NP_059989.3:p.Pro1669Gln