Canonical Allele Identifier: CA366242872

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376476
• MyVariant Identifiers: chr6:g.157522522A>T (hg19) ; chr6:g.157201388A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201388A>T , CM000668.2:g.157201388A>T	GRCh38
NC_000006.11:g.157522522A>T , CM000668.1:g.157522522A>T	GRCh37
NC_000006.10:g.157564214A>T	NCBI36
NG_032093.1:g.428459A>T
NG_032093.2:g.428459A>T
NG_066624.1:g.430363A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5004A>T	ENSP00000055163.8:p.Gln1668His
ENST00000414678.8:c.5073A>T	ENSP00000412835.3:p.Gln1691His
ENST00000637015.2:c.5292A>T	ENSP00000489729.2:p.Gln1764His
ENST00000346085.10:c.5043A>T	ENSP00000344546.5:p.Gln1681His
ENST00000350026.10:c.4755A>T	ENSP00000055163.7:p.Gln1585His
ENST00000414678.7:c.3321A>T	ENSP00000412835.2:p.Gln1107His
ENST00000635849.1:c.2484A>T	ENSP00000490948.1:p.Gln828His
ENST00000635957.1:c.2115A>T	ENSP00000490385.1:p.Gln705His
ENST00000636227.1:n.3626A>T
ENST00000636254.1:n.1083A>T
ENST00000636930.2:c.5163A>T MANE Select	ENSP00000490491.2:p.Gln1721His
ENST00000636940.1:n.3160A>T
ENST00000637015.1:c.2531A>T
ENST00000637568.1:c.2445A>T
ENST00000637741.1:n.1829A>T
ENST00000637810.1:c.2505A>T	ENSP00000489636.1:p.Gln835His
ENST00000637904.1:c.2664A>T	ENSP00000490550.1:p.Gln888His
ENST00000647938.1:c.4794A>T	ENSP00000498155.1:p.Gln1598His
ENST00000346085.9:c.4794A>T	ENSP00000344546.4:p.Gln1598His
ENST00000350026.9:c.4755A>T	ENSP00000055163.7:p.Gln1585His
ENST00000414678.6:c.3321A>T	ENSP00000412835.2:p.Gln1107His
NM_017519.2:c.4755A>T	NP_059989.2:p.Gln1585His
NM_020732.3:c.4794A>T	NP_065783.3:p.Gln1598His
XM_005267069.3:c.4914A>T	XP_005267126.2:p.Gln1638His
XM_011535984.1:c.3993A>T	XP_011534286.1:p.Gln1331His
XM_011535985.1:c.3813A>T	XP_011534287.1:p.Gln1271His
XM_011535986.1:c.3573A>T	XP_011534288.1:p.Gln1191His
XM_011535987.1:c.3192A>T	XP_011534289.1:p.Gln1064His
XM_011535988.1:c.2055A>T	XP_011534290.1:p.Gln685His
NM_001346813.1:c.4914A>T	NP_001333742.1:p.Gln1638His
NM_001363725.1:c.2664A>T	NP_001350654.1:p.Gln888His
XM_011535984.2:c.5124A>T	XP_011534286.2:p.Gln1708His
XM_011535988.3:c.2055A>T	XP_011534290.1:p.Gln685His
XM_017011103.2:c.5025A>T	XP_016866592.1:p.Gln1675His
XM_017011104.1:c.4995A>T	XP_016866593.1:p.Gln1665His
XM_017011105.2:c.4965A>T	XP_016866594.1:p.Gln1655His
XM_017011106.2:c.4836A>T	XP_016866595.1:p.Gln1612His
XM_017011107.2:c.4815A>T	XP_016866596.1:p.Gln1605His
XR_002956289.1:n.5110A>T
NM_001363725.2:c.2664A>T	NP_001350654.1:p.Gln888His
NM_001371656.1:c.5043A>T	NP_001358585.1:p.Gln1681His
NM_001374820.1:c.5043A>T	NP_001361749.1:p.Gln1681His
NM_001374828.1:c.5163A>T MANE Select	NP_001361757.1:p.Gln1721His
NM_017519.3:c.5004A>T	NP_059989.3:p.Gln1668His