Canonical Allele Identifier: CA366235271

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511237A>T (hg19) ; chr6:g.157190103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190103A>T , CM000668.2:g.157190103A>T	GRCh38
NC_000006.11:g.157511237A>T , CM000668.1:g.157511237A>T	GRCh37
NC_000006.10:g.157552929A>T	NCBI36
NG_032093.1:g.417174A>T
NG_032093.2:g.417174A>T
NG_066624.1:g.419078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3965A>T	ENSP00000055163.8:p.Asn1322Ile
ENST00000414678.8:c.4034A>T	ENSP00000412835.3:p.Asn1345Ile
ENST00000637015.2:c.4253A>T	ENSP00000489729.2:p.Asn1418Ile
ENST00000346085.10:c.4004A>T	ENSP00000344546.5:p.Asn1335Ile
ENST00000350026.10:c.3716A>T	ENSP00000055163.7:p.Asn1239Ile
ENST00000414678.7:c.2282A>T	ENSP00000412835.2:p.Asn761Ile
ENST00000635849.1:c.1445A>T	ENSP00000490948.1:p.Asn482Ile
ENST00000635957.1:c.1076A>T	ENSP00000490385.1:p.Asn359Ile
ENST00000636930.2:c.4124A>T MANE Select	ENSP00000490491.2:p.Asn1375Ile
ENST00000636940.1:n.2121A>T
ENST00000637015.1:c.1492A>T
ENST00000637568.1:c.1406A>T
ENST00000637741.1:n.790A>T
ENST00000637810.1:c.1466A>T	ENSP00000489636.1:p.Asn489Ile
ENST00000637904.1:c.1625A>T	ENSP00000490550.1:p.Asn542Ile
ENST00000647938.1:c.3755A>T	ENSP00000498155.1:p.Asn1252Ile
ENST00000346085.9:c.3755A>T	ENSP00000344546.4:p.Asn1252Ile
ENST00000350026.9:c.3716A>T	ENSP00000055163.7:p.Asn1239Ile
ENST00000414678.6:c.2282A>T	ENSP00000412835.2:p.Asn761Ile
NM_017519.2:c.3716A>T	NP_059989.2:p.Asn1239Ile
NM_020732.3:c.3755A>T	NP_065783.3:p.Asn1252Ile
XM_005267069.3:c.3875A>T	XP_005267126.2:p.Asn1292Ile
XM_011535984.1:c.2954A>T	XP_011534286.1:p.Asn985Ile
XM_011535985.1:c.2774A>T	XP_011534287.1:p.Asn925Ile
XM_011535986.1:c.2534A>T	XP_011534288.1:p.Asn845Ile
XM_011535987.1:c.2153A>T	XP_011534289.1:p.Asn718Ile
XM_011535988.1:c.1016A>T	XP_011534290.1:p.Asn339Ile
NM_001346813.1:c.3875A>T	NP_001333742.1:p.Asn1292Ile
NM_001363725.1:c.1625A>T	NP_001350654.1:p.Asn542Ile
XM_011535984.2:c.4085A>T	XP_011534286.2:p.Asn1362Ile
XM_011535988.3:c.1016A>T	XP_011534290.1:p.Asn339Ile
XM_017011103.2:c.3986A>T	XP_016866592.1:p.Asn1329Ile
XM_017011104.1:c.3956A>T	XP_016866593.1:p.Asn1319Ile
XM_017011105.2:c.3926A>T	XP_016866594.1:p.Asn1309Ile
XM_017011106.2:c.3797A>T	XP_016866595.1:p.Asn1266Ile
XM_017011107.2:c.3776A>T	XP_016866596.1:p.Asn1259Ile
XR_002956289.1:n.4168A>T
NM_001363725.2:c.1625A>T	NP_001350654.1:p.Asn542Ile
NM_001371656.1:c.4004A>T	NP_001358585.1:p.Asn1335Ile
NM_001374820.1:c.4004A>T	NP_001361749.1:p.Asn1335Ile
NM_001374828.1:c.4124A>T MANE Select	NP_001361757.1:p.Asn1375Ile
NM_017519.3:c.3965A>T	NP_059989.3:p.Asn1322Ile