Canonical Allele Identifier: CA366235308

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511252A>T (hg19) ; chr6:g.157190118A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190118A>T , CM000668.2:g.157190118A>T	GRCh38
NC_000006.11:g.157511252A>T , CM000668.1:g.157511252A>T	GRCh37
NC_000006.10:g.157552944A>T	NCBI36
NG_032093.1:g.417189A>T
NG_032093.2:g.417189A>T
NG_066624.1:g.419093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3980A>T	ENSP00000055163.8:p.Asn1327Ile
ENST00000414678.8:c.4049A>T	ENSP00000412835.3:p.Asn1350Ile
ENST00000637015.2:c.4268A>T	ENSP00000489729.2:p.Asn1423Ile
ENST00000346085.10:c.4019A>T	ENSP00000344546.5:p.Asn1340Ile
ENST00000350026.10:c.3731A>T	ENSP00000055163.7:p.Asn1244Ile
ENST00000414678.7:c.2297A>T	ENSP00000412835.2:p.Asn766Ile
ENST00000635849.1:c.1460A>T	ENSP00000490948.1:p.Asn487Ile
ENST00000635957.1:c.1091A>T	ENSP00000490385.1:p.Asn364Ile
ENST00000636930.2:c.4139A>T MANE Select	ENSP00000490491.2:p.Asn1380Ile
ENST00000636940.1:n.2136A>T
ENST00000637015.1:c.1507A>T
ENST00000637568.1:c.1421A>T
ENST00000637741.1:n.805A>T
ENST00000637810.1:c.1481A>T	ENSP00000489636.1:p.Asn494Ile
ENST00000637904.1:c.1640A>T	ENSP00000490550.1:p.Asn547Ile
ENST00000647938.1:c.3770A>T	ENSP00000498155.1:p.Asn1257Ile
ENST00000346085.9:c.3770A>T	ENSP00000344546.4:p.Asn1257Ile
ENST00000350026.9:c.3731A>T	ENSP00000055163.7:p.Asn1244Ile
ENST00000414678.6:c.2297A>T	ENSP00000412835.2:p.Asn766Ile
NM_017519.2:c.3731A>T	NP_059989.2:p.Asn1244Ile
NM_020732.3:c.3770A>T	NP_065783.3:p.Asn1257Ile
XM_005267069.3:c.3890A>T	XP_005267126.2:p.Asn1297Ile
XM_011535984.1:c.2969A>T	XP_011534286.1:p.Asn990Ile
XM_011535985.1:c.2789A>T	XP_011534287.1:p.Asn930Ile
XM_011535986.1:c.2549A>T	XP_011534288.1:p.Asn850Ile
XM_011535987.1:c.2168A>T	XP_011534289.1:p.Asn723Ile
XM_011535988.1:c.1031A>T	XP_011534290.1:p.Asn344Ile
NM_001346813.1:c.3890A>T	NP_001333742.1:p.Asn1297Ile
NM_001363725.1:c.1640A>T	NP_001350654.1:p.Asn547Ile
XM_011535984.2:c.4100A>T	XP_011534286.2:p.Asn1367Ile
XM_011535988.3:c.1031A>T	XP_011534290.1:p.Asn344Ile
XM_017011103.2:c.4001A>T	XP_016866592.1:p.Asn1334Ile
XM_017011104.1:c.3971A>T	XP_016866593.1:p.Asn1324Ile
XM_017011105.2:c.3941A>T	XP_016866594.1:p.Asn1314Ile
XM_017011106.2:c.3812A>T	XP_016866595.1:p.Asn1271Ile
XM_017011107.2:c.3791A>T	XP_016866596.1:p.Asn1264Ile
XR_002956289.1:n.4183A>T
NM_001363725.2:c.1640A>T	NP_001350654.1:p.Asn547Ile
NM_001371656.1:c.4019A>T	NP_001358585.1:p.Asn1340Ile
NM_001374820.1:c.4019A>T	NP_001361749.1:p.Asn1340Ile
NM_001374828.1:c.4139A>T MANE Select	NP_001361757.1:p.Asn1380Ile
NM_017519.3:c.3980A>T	NP_059989.3:p.Asn1327Ile