Canonical Allele Identifier: CA366241176

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373253
• MyVariant Identifiers: chr6:g.157522029G>A (hg19) ; chr6:g.157200895G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200895G>A , CM000668.2:g.157200895G>A	GRCh38
NC_000006.11:g.157522029G>A , CM000668.1:g.157522029G>A	GRCh37
NC_000006.10:g.157563721G>A	NCBI36
NG_032093.1:g.427966G>A
NG_032093.2:g.427966G>A
NG_066624.1:g.429870G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4511G>A	ENSP00000055163.8:p.Gly1504Asp
ENST00000414678.8:c.4580G>A	ENSP00000412835.3:p.Gly1527Asp
ENST00000637015.2:c.4799G>A	ENSP00000489729.2:p.Gly1600Asp
ENST00000346085.10:c.4550G>A	ENSP00000344546.5:p.Gly1517Asp
ENST00000350026.10:c.4262G>A	ENSP00000055163.7:p.Gly1421Asp
ENST00000414678.7:c.2828G>A	ENSP00000412835.2:p.Gly943Asp
ENST00000635849.1:c.1991G>A	ENSP00000490948.1:p.Gly664Asp
ENST00000635957.1:c.1622G>A	ENSP00000490385.1:p.Gly541Asp
ENST00000636227.1:n.3133G>A
ENST00000636254.1:n.590G>A
ENST00000636930.2:c.4670G>A MANE Select	ENSP00000490491.2:p.Gly1557Asp
ENST00000636940.1:n.2667G>A
ENST00000637015.1:c.2038G>A
ENST00000637568.1:c.1952G>A
ENST00000637741.1:n.1336G>A
ENST00000637810.1:c.2012G>A	ENSP00000489636.1:p.Gly671Asp
ENST00000637904.1:c.2171G>A	ENSP00000490550.1:p.Gly724Asp
ENST00000647938.1:c.4301G>A	ENSP00000498155.1:p.Gly1434Asp
ENST00000346085.9:c.4301G>A	ENSP00000344546.4:p.Gly1434Asp
ENST00000350026.9:c.4262G>A	ENSP00000055163.7:p.Gly1421Asp
ENST00000414678.6:c.2828G>A	ENSP00000412835.2:p.Gly943Asp
NM_017519.2:c.4262G>A	NP_059989.2:p.Gly1421Asp
NM_020732.3:c.4301G>A	NP_065783.3:p.Gly1434Asp
XM_005267069.3:c.4421G>A	XP_005267126.2:p.Gly1474Asp
XM_011535984.1:c.3500G>A	XP_011534286.1:p.Gly1167Asp
XM_011535985.1:c.3320G>A	XP_011534287.1:p.Gly1107Asp
XM_011535986.1:c.3080G>A	XP_011534288.1:p.Gly1027Asp
XM_011535987.1:c.2699G>A	XP_011534289.1:p.Gly900Asp
XM_011535988.1:c.1562G>A	XP_011534290.1:p.Gly521Asp
NM_001346813.1:c.4421G>A	NP_001333742.1:p.Gly1474Asp
NM_001363725.1:c.2171G>A	NP_001350654.1:p.Gly724Asp
XM_011535984.2:c.4631G>A	XP_011534286.2:p.Gly1544Asp
XM_011535988.3:c.1562G>A	XP_011534290.1:p.Gly521Asp
XM_017011103.2:c.4532G>A	XP_016866592.1:p.Gly1511Asp
XM_017011104.1:c.4502G>A	XP_016866593.1:p.Gly1501Asp
XM_017011105.2:c.4472G>A	XP_016866594.1:p.Gly1491Asp
XM_017011106.2:c.4343G>A	XP_016866595.1:p.Gly1448Asp
XM_017011107.2:c.4322G>A	XP_016866596.1:p.Gly1441Asp
XR_002956289.1:n.4617G>A
NM_001363725.2:c.2171G>A	NP_001350654.1:p.Gly724Asp
NM_001371656.1:c.4550G>A	NP_001358585.1:p.Gly1517Asp
NM_001374820.1:c.4550G>A	NP_001361749.1:p.Gly1517Asp
NM_001374828.1:c.4670G>A MANE Select	NP_001361757.1:p.Gly1557Asp
NM_017519.3:c.4511G>A	NP_059989.3:p.Gly1504Asp