Canonical Allele Identifier: CA452978397

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522180T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201046T>G , CM000668.2:g.157201046T>G	GRCh38
NC_000006.11:g.157522180T>G , CM000668.1:g.157522180T>G	GRCh37
NC_000006.10:g.157563872T>G	NCBI36
NG_032093.1:g.428117T>G
NG_032093.2:g.428117T>G
NG_066624.1:g.430021T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4662T>G	ENSP00000055163.8:p.Pro1554=
ENST00000414678.8:c.4731T>G	ENSP00000412835.3:p.Pro1577=
ENST00000637015.2:c.4950T>G	ENSP00000489729.2:p.Pro1650=
ENST00000346085.10:c.4701T>G	ENSP00000344546.5:p.Pro1567=
ENST00000350026.10:c.4413T>G	ENSP00000055163.7:p.Pro1471=
ENST00000414678.7:c.2979T>G	ENSP00000412835.2:p.Pro993=
ENST00000635849.1:c.2142T>G	ENSP00000490948.1:p.Pro714=
ENST00000635957.1:c.1773T>G	ENSP00000490385.1:p.Pro591=
ENST00000636227.1:n.3284T>G
ENST00000636254.1:n.741T>G
ENST00000636930.2:c.4821T>G MANE Select	ENSP00000490491.2:p.Pro1607=
ENST00000636940.1:n.2818T>G
ENST00000637015.1:c.2189T>G
ENST00000637568.1:c.2103T>G
ENST00000637741.1:n.1487T>G
ENST00000637810.1:c.2163T>G	ENSP00000489636.1:p.Pro721=
ENST00000637904.1:c.2322T>G	ENSP00000490550.1:p.Pro774=
ENST00000647938.1:c.4452T>G	ENSP00000498155.1:p.Pro1484=
ENST00000346085.9:c.4452T>G	ENSP00000344546.4:p.Pro1484=
ENST00000350026.9:c.4413T>G	ENSP00000055163.7:p.Pro1471=
ENST00000414678.6:c.2979T>G	ENSP00000412835.2:p.Pro993=
NM_017519.2:c.4413T>G	NP_059989.2:p.Pro1471=
NM_020732.3:c.4452T>G	NP_065783.3:p.Pro1484=
XM_005267069.3:c.4572T>G	XP_005267126.2:p.Pro1524=
XM_011535984.1:c.3651T>G	XP_011534286.1:p.Pro1217=
XM_011535985.1:c.3471T>G	XP_011534287.1:p.Pro1157=
XM_011535986.1:c.3231T>G	XP_011534288.1:p.Pro1077=
XM_011535987.1:c.2850T>G	XP_011534289.1:p.Pro950=
XM_011535988.1:c.1713T>G	XP_011534290.1:p.Pro571=
NM_001346813.1:c.4572T>G	NP_001333742.1:p.Pro1524=
NM_001363725.1:c.2322T>G	NP_001350654.1:p.Pro774=
XM_011535984.2:c.4782T>G	XP_011534286.2:p.Pro1594=
XM_011535988.3:c.1713T>G	XP_011534290.1:p.Pro571=
XM_017011103.2:c.4683T>G	XP_016866592.1:p.Pro1561=
XM_017011104.1:c.4653T>G	XP_016866593.1:p.Pro1551=
XM_017011105.2:c.4623T>G	XP_016866594.1:p.Pro1541=
XM_017011106.2:c.4494T>G	XP_016866595.1:p.Pro1498=
XM_017011107.2:c.4473T>G	XP_016866596.1:p.Pro1491=
XR_002956289.1:n.4768T>G
NM_001363725.2:c.2322T>G	NP_001350654.1:p.Pro774=
NM_001371656.1:c.4701T>G	NP_001358585.1:p.Pro1567=
NM_001374820.1:c.4701T>G	NP_001361749.1:p.Pro1567=
NM_001374828.1:c.4821T>G MANE Select	NP_001361757.1:p.Pro1607=
NM_017519.3:c.4662T>G	NP_059989.3:p.Pro1554=