Canonical Allele Identifier: CA452977892

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200875-C-T
• MyVariant Identifiers: chr6:g.157522009C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200875C>T , CM000668.2:g.157200875C>T	GRCh38
NC_000006.11:g.157522009C>T , CM000668.1:g.157522009C>T	GRCh37
NC_000006.10:g.157563701C>T	NCBI36
NG_032093.1:g.427946C>T
NG_032093.2:g.427946C>T
NG_066624.1:g.429850C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4491C>T	ENSP00000055163.8:p.Tyr1497=
ENST00000414678.8:c.4560C>T	ENSP00000412835.3:p.Tyr1520=
ENST00000637015.2:c.4779C>T	ENSP00000489729.2:p.Tyr1593=
ENST00000346085.10:c.4530C>T	ENSP00000344546.5:p.Tyr1510=
ENST00000350026.10:c.4242C>T	ENSP00000055163.7:p.Tyr1414=
ENST00000414678.7:c.2808C>T	ENSP00000412835.2:p.Tyr936=
ENST00000635849.1:c.1971C>T	ENSP00000490948.1:p.Tyr657=
ENST00000635957.1:c.1602C>T	ENSP00000490385.1:p.Tyr534=
ENST00000636227.1:n.3113C>T
ENST00000636254.1:n.570C>T
ENST00000636930.2:c.4650C>T MANE Select	ENSP00000490491.2:p.Tyr1550=
ENST00000636940.1:n.2647C>T
ENST00000637015.1:c.2018C>T
ENST00000637568.1:c.1932C>T
ENST00000637741.1:n.1316C>T
ENST00000637810.1:c.1992C>T	ENSP00000489636.1:p.Tyr664=
ENST00000637904.1:c.2151C>T	ENSP00000490550.1:p.Tyr717=
ENST00000647938.1:c.4281C>T	ENSP00000498155.1:p.Tyr1427=
ENST00000346085.9:c.4281C>T	ENSP00000344546.4:p.Tyr1427=
ENST00000350026.9:c.4242C>T	ENSP00000055163.7:p.Tyr1414=
ENST00000414678.6:c.2808C>T	ENSP00000412835.2:p.Tyr936=
NM_017519.2:c.4242C>T	NP_059989.2:p.Tyr1414=
NM_020732.3:c.4281C>T	NP_065783.3:p.Tyr1427=
XM_005267069.3:c.4401C>T	XP_005267126.2:p.Tyr1467=
XM_011535984.1:c.3480C>T	XP_011534286.1:p.Tyr1160=
XM_011535985.1:c.3300C>T	XP_011534287.1:p.Tyr1100=
XM_011535986.1:c.3060C>T	XP_011534288.1:p.Tyr1020=
XM_011535987.1:c.2679C>T	XP_011534289.1:p.Tyr893=
XM_011535988.1:c.1542C>T	XP_011534290.1:p.Tyr514=
NM_001346813.1:c.4401C>T	NP_001333742.1:p.Tyr1467=
NM_001363725.1:c.2151C>T	NP_001350654.1:p.Tyr717=
XM_011535984.2:c.4611C>T	XP_011534286.2:p.Tyr1537=
XM_011535988.3:c.1542C>T	XP_011534290.1:p.Tyr514=
XM_017011103.2:c.4512C>T	XP_016866592.1:p.Tyr1504=
XM_017011104.1:c.4482C>T	XP_016866593.1:p.Tyr1494=
XM_017011105.2:c.4452C>T	XP_016866594.1:p.Tyr1484=
XM_017011106.2:c.4323C>T	XP_016866595.1:p.Tyr1441=
XM_017011107.2:c.4302C>T	XP_016866596.1:p.Tyr1434=
XR_002956289.1:n.4597C>T
NM_001363725.2:c.2151C>T	NP_001350654.1:p.Tyr717=
NM_001371656.1:c.4530C>T	NP_001358585.1:p.Tyr1510=
NM_001374820.1:c.4530C>T	NP_001361749.1:p.Tyr1510=
NM_001374828.1:c.4650C>T MANE Select	NP_001361757.1:p.Tyr1550=
NM_017519.3:c.4491C>T	NP_059989.3:p.Tyr1497=