Canonical Allele Identifier: CA366234050

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189669-A-C
• MyVariant Identifiers: chr6:g.157510803A>C (hg19) ; chr6:g.157189669A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189669A>C , CM000668.2:g.157189669A>C	GRCh38
NC_000006.11:g.157510803A>C , CM000668.1:g.157510803A>C	GRCh37
NC_000006.10:g.157552495A>C	NCBI36
NG_032093.1:g.416740A>C
NG_032093.2:g.416740A>C
NG_066624.1:g.418644A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3788A>C	ENSP00000055163.8:p.Gln1263Pro
ENST00000414678.8:c.3857A>C	ENSP00000412835.3:p.Gln1286Pro
ENST00000637015.2:c.4076A>C	ENSP00000489729.2:p.Gln1359Pro
ENST00000346085.10:c.3827A>C	ENSP00000344546.5:p.Gln1276Pro
ENST00000350026.10:c.3539A>C	ENSP00000055163.7:p.Gln1180Pro
ENST00000414678.7:c.2105A>C	ENSP00000412835.2:p.Gln702Pro
ENST00000635849.1:c.1268A>C	ENSP00000490948.1:p.Gln423Pro
ENST00000635957.1:c.902A>C	ENSP00000490385.1:p.Gln301Pro
ENST00000636930.2:c.3947A>C MANE Select	ENSP00000490491.2:p.Gln1316Pro
ENST00000636940.1:n.1944A>C
ENST00000637015.1:c.1315A>C
ENST00000637568.1:c.1229A>C
ENST00000637741.1:n.613A>C
ENST00000637810.1:c.1289A>C	ENSP00000489636.1:p.Gln430Pro
ENST00000637904.1:c.1448A>C	ENSP00000490550.1:p.Gln483Pro
ENST00000647938.1:c.3578A>C	ENSP00000498155.1:p.Gln1193Pro
ENST00000346085.9:c.3578A>C	ENSP00000344546.4:p.Gln1193Pro
ENST00000350026.9:c.3539A>C	ENSP00000055163.7:p.Gln1180Pro
ENST00000414678.6:c.2105A>C	ENSP00000412835.2:p.Gln702Pro
NM_017519.2:c.3539A>C	NP_059989.2:p.Gln1180Pro
NM_020732.3:c.3578A>C	NP_065783.3:p.Gln1193Pro
XM_005267069.3:c.3698A>C	XP_005267126.2:p.Gln1233Pro
XM_011535984.1:c.2777A>C	XP_011534286.1:p.Gln926Pro
XM_011535985.1:c.2597A>C	XP_011534287.1:p.Gln866Pro
XM_011535986.1:c.2357A>C	XP_011534288.1:p.Gln786Pro
XM_011535987.1:c.1976A>C	XP_011534289.1:p.Gln659Pro
XM_011535988.1:c.839A>C	XP_011534290.1:p.Gln280Pro
NM_001346813.1:c.3698A>C	NP_001333742.1:p.Gln1233Pro
NM_001363725.1:c.1448A>C	NP_001350654.1:p.Gln483Pro
XM_011535984.2:c.3908A>C	XP_011534286.2:p.Gln1303Pro
XM_011535988.3:c.839A>C	XP_011534290.1:p.Gln280Pro
XM_017011103.2:c.3809A>C	XP_016866592.1:p.Gln1270Pro
XM_017011104.1:c.3779A>C	XP_016866593.1:p.Gln1260Pro
XM_017011105.2:c.3749A>C	XP_016866594.1:p.Gln1250Pro
XM_017011106.2:c.3620A>C	XP_016866595.1:p.Gln1207Pro
XM_017011107.2:c.3599A>C	XP_016866596.1:p.Gln1200Pro
XR_002956289.1:n.3991A>C
NM_001363725.2:c.1448A>C	NP_001350654.1:p.Gln483Pro
NM_001371656.1:c.3827A>C	NP_001358585.1:p.Gln1276Pro
NM_001374820.1:c.3827A>C	NP_001361749.1:p.Gln1276Pro
NM_001374828.1:c.3947A>C MANE Select	NP_001361757.1:p.Gln1316Pro
NM_017519.3:c.3788A>C	NP_059989.3:p.Gln1263Pro