Canonical Allele Identifier: CA366239666

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366135
• gnomAD v4: 6-157198844-A-C
• MyVariant Identifiers: chr6:g.157519978A>C (hg19) ; chr6:g.157198844A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198844A>C , CM000668.2:g.157198844A>C	GRCh38
NC_000006.11:g.157519978A>C , CM000668.1:g.157519978A>C	GRCh37
NC_000006.10:g.157561670A>C	NCBI36
NG_032093.1:g.425915A>C
NG_032093.2:g.425915A>C
NG_066624.1:g.427819A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4257A>C	ENSP00000055163.8:p.Gln1419His
ENST00000414678.8:c.4326A>C	ENSP00000412835.3:p.Gln1442His
ENST00000637015.2:c.4545A>C	ENSP00000489729.2:p.Gln1515His
ENST00000346085.10:c.4296A>C	ENSP00000344546.5:p.Gln1432His
ENST00000350026.10:c.4008A>C	ENSP00000055163.7:p.Gln1336His
ENST00000414678.7:c.2574A>C	ENSP00000412835.2:p.Gln858His
ENST00000635849.1:c.1737A>C	ENSP00000490948.1:p.Gln579His
ENST00000635957.1:c.1368A>C	ENSP00000490385.1:p.Gln456His
ENST00000636227.1:n.2879A>C
ENST00000636254.1:n.336A>C
ENST00000636930.2:c.4416A>C MANE Select	ENSP00000490491.2:p.Gln1472His
ENST00000636940.1:n.2413A>C
ENST00000637015.1:c.1784A>C
ENST00000637568.1:c.1698A>C
ENST00000637741.1:n.1082A>C
ENST00000637810.1:c.1758A>C	ENSP00000489636.1:p.Gln586His
ENST00000637904.1:c.1917A>C	ENSP00000490550.1:p.Gln639His
ENST00000647938.1:c.4047A>C	ENSP00000498155.1:p.Gln1349His
ENST00000346085.9:c.4047A>C	ENSP00000344546.4:p.Gln1349His
ENST00000350026.9:c.4008A>C	ENSP00000055163.7:p.Gln1336His
ENST00000414678.6:c.2574A>C	ENSP00000412835.2:p.Gln858His
NM_017519.2:c.4008A>C	NP_059989.2:p.Gln1336His
NM_020732.3:c.4047A>C	NP_065783.3:p.Gln1349His
XM_005267069.3:c.4167A>C	XP_005267126.2:p.Gln1389His
XM_011535984.1:c.3246A>C	XP_011534286.1:p.Gln1082His
XM_011535985.1:c.3066A>C	XP_011534287.1:p.Gln1022His
XM_011535986.1:c.2826A>C	XP_011534288.1:p.Gln942His
XM_011535987.1:c.2445A>C	XP_011534289.1:p.Gln815His
XM_011535988.1:c.1308A>C	XP_011534290.1:p.Gln436His
NM_001346813.1:c.4167A>C	NP_001333742.1:p.Gln1389His
NM_001363725.1:c.1917A>C	NP_001350654.1:p.Gln639His
XM_011535984.2:c.4377A>C	XP_011534286.2:p.Gln1459His
XM_011535988.3:c.1308A>C	XP_011534290.1:p.Gln436His
XM_017011103.2:c.4278A>C	XP_016866592.1:p.Gln1426His
XM_017011104.1:c.4248A>C	XP_016866593.1:p.Gln1416His
XM_017011105.2:c.4218A>C	XP_016866594.1:p.Gln1406His
XM_017011106.2:c.4089A>C	XP_016866595.1:p.Gln1363His
XM_017011107.2:c.4068A>C	XP_016866596.1:p.Gln1356His
XR_002956289.1:n.4427-1861A>C
NM_001363725.2:c.1917A>C	NP_001350654.1:p.Gln639His
NM_001371656.1:c.4296A>C	NP_001358585.1:p.Gln1432His
NM_001374820.1:c.4296A>C	NP_001361749.1:p.Gln1432His
NM_001374828.1:c.4416A>C MANE Select	NP_001361757.1:p.Gln1472His
NM_017519.3:c.4257A>C	NP_059989.3:p.Gln1419His