Canonical Allele Identifier: CA366240911

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521912A>T (hg19) ; chr6:g.157200778A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200778A>T , CM000668.2:g.157200778A>T	GRCh38
NC_000006.11:g.157521912A>T , CM000668.1:g.157521912A>T	GRCh37
NC_000006.10:g.157563604A>T	NCBI36
NG_032093.1:g.427849A>T
NG_032093.2:g.427849A>T
NG_066624.1:g.429753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4394A>T	ENSP00000055163.8:p.Gln1465Leu
ENST00000414678.8:c.4463A>T	ENSP00000412835.3:p.Gln1488Leu
ENST00000637015.2:c.4682A>T	ENSP00000489729.2:p.Gln1561Leu
ENST00000346085.10:c.4433A>T	ENSP00000344546.5:p.Gln1478Leu
ENST00000350026.10:c.4145A>T	ENSP00000055163.7:p.Gln1382Leu
ENST00000414678.7:c.2711A>T	ENSP00000412835.2:p.Gln904Leu
ENST00000635849.1:c.1874A>T	ENSP00000490948.1:p.Gln625Leu
ENST00000635957.1:c.1505A>T	ENSP00000490385.1:p.Gln502Leu
ENST00000636227.1:n.3016A>T
ENST00000636254.1:n.473A>T
ENST00000636930.2:c.4553A>T MANE Select	ENSP00000490491.2:p.Gln1518Leu
ENST00000636940.1:n.2550A>T
ENST00000637015.1:c.1921A>T
ENST00000637568.1:c.1835A>T
ENST00000637741.1:n.1219A>T
ENST00000637810.1:c.1895A>T	ENSP00000489636.1:p.Gln632Leu
ENST00000637904.1:c.2054A>T	ENSP00000490550.1:p.Gln685Leu
ENST00000647938.1:c.4184A>T	ENSP00000498155.1:p.Gln1395Leu
ENST00000346085.9:c.4184A>T	ENSP00000344546.4:p.Gln1395Leu
ENST00000350026.9:c.4145A>T	ENSP00000055163.7:p.Gln1382Leu
ENST00000414678.6:c.2711A>T	ENSP00000412835.2:p.Gln904Leu
NM_017519.2:c.4145A>T	NP_059989.2:p.Gln1382Leu
NM_020732.3:c.4184A>T	NP_065783.3:p.Gln1395Leu
XM_005267069.3:c.4304A>T	XP_005267126.2:p.Gln1435Leu
XM_011535984.1:c.3383A>T	XP_011534286.1:p.Gln1128Leu
XM_011535985.1:c.3203A>T	XP_011534287.1:p.Gln1068Leu
XM_011535986.1:c.2963A>T	XP_011534288.1:p.Gln988Leu
XM_011535987.1:c.2582A>T	XP_011534289.1:p.Gln861Leu
XM_011535988.1:c.1445A>T	XP_011534290.1:p.Gln482Leu
NM_001346813.1:c.4304A>T	NP_001333742.1:p.Gln1435Leu
NM_001363725.1:c.2054A>T	NP_001350654.1:p.Gln685Leu
XM_011535984.2:c.4514A>T	XP_011534286.2:p.Gln1505Leu
XM_011535988.3:c.1445A>T	XP_011534290.1:p.Gln482Leu
XM_017011103.2:c.4415A>T	XP_016866592.1:p.Gln1472Leu
XM_017011104.1:c.4385A>T	XP_016866593.1:p.Gln1462Leu
XM_017011105.2:c.4355A>T	XP_016866594.1:p.Gln1452Leu
XM_017011106.2:c.4226A>T	XP_016866595.1:p.Gln1409Leu
XM_017011107.2:c.4205A>T	XP_016866596.1:p.Gln1402Leu
XR_002956289.1:n.4500A>T
NM_001363725.2:c.2054A>T	NP_001350654.1:p.Gln685Leu
NM_001371656.1:c.4433A>T	NP_001358585.1:p.Gln1478Leu
NM_001374820.1:c.4433A>T	NP_001361749.1:p.Gln1478Leu
NM_001374828.1:c.4553A>T MANE Select	NP_001361757.1:p.Gln1518Leu
NM_017519.3:c.4394A>T	NP_059989.3:p.Gln1465Leu