Canonical Allele Identifier: CA366389176

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470022A>T (hg19) ; chr6:g.157148888A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148888A>T , CM000668.2:g.157148888A>T	GRCh38
NC_000006.11:g.157470022A>T , CM000668.1:g.157470022A>T	GRCh37
NC_000006.10:g.157511714A>T	NCBI36
NG_032093.1:g.375959A>T
NG_032093.2:g.375959A>T
NG_066624.1:g.377863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3026A>T	ENSP00000055163.8:p.Asn1009Ile
ENST00000414678.8:c.2936A>T	ENSP00000412835.3:p.Asn979Ile
ENST00000637015.2:c.3026A>T	ENSP00000489729.2:p.Asn1009Ile
ENST00000319584.11:c.1040A>T	ENSP00000313006.7:p.Asn347Ile
ENST00000346085.10:c.3065A>T	ENSP00000344546.5:p.Asn1022Ile
ENST00000350026.10:c.2777A>T	ENSP00000055163.7:p.Asn926Ile
ENST00000414678.7:c.1184A>T	ENSP00000412835.2:p.Asn395Ile
ENST00000452544.2:n.927A>T
ENST00000635849.1:c.347A>T	ENSP00000490948.1:p.Asn116Ile
ENST00000636426.1:n.160A>T
ENST00000636930.2:c.3026A>T MANE Select	ENSP00000490491.2:p.Asn1009Ile
ENST00000637015.1:c.265A>T
ENST00000637568.1:c.69A>T
ENST00000637810.1:c.527A>T	ENSP00000489636.1:p.Asn176Ile
ENST00000637904.1:c.527A>T	ENSP00000490550.1:p.Asn176Ile
ENST00000647938.1:c.2816A>T	ENSP00000498155.1:p.Asn939Ile
ENST00000674190.1:n.1775A>T
ENST00000319584.10:c.1043A>T	ENSP00000313006.6:p.Asn348Ile
ENST00000346085.9:c.2816A>T	ENSP00000344546.4:p.Asn939Ile
ENST00000350026.9:c.2777A>T	ENSP00000055163.7:p.Asn926Ile
ENST00000414678.6:c.1184A>T	ENSP00000412835.2:p.Asn395Ile
ENST00000452544.1:n.873A>T
ENST00000478761.3:c.99A>T
NM_017519.2:c.2777A>T	NP_059989.2:p.Asn926Ile
NM_020732.3:c.2816A>T	NP_065783.3:p.Asn939Ile
XM_005267069.3:c.2777A>T	XP_005267126.2:p.Asn926Ile
XM_011535984.1:c.1727A>T	XP_011534286.1:p.Asn576Ile
XM_011535985.1:c.1547A>T	XP_011534287.1:p.Asn516Ile
XM_011535986.1:c.1307A>T	XP_011534288.1:p.Asn436Ile
XM_011535987.1:c.926A>T	XP_011534289.1:p.Asn309Ile
XM_011535988.1:c.-20+15681A>T	XP_011534290.1:n.-20+15681A>T
NM_001346813.1:c.2777A>T	NP_001333742.1:p.Asn926Ile
NM_001363725.1:c.527A>T	NP_001350654.1:p.Asn176Ile
XM_011535984.2:c.2858A>T	XP_011534286.2:p.Asn953Ile
XM_011535988.3:c.-20+15681A>T	XP_011534290.1:n.-20+15681A>T
XM_017011103.2:c.2858A>T	XP_016866592.1:p.Asn953Ile
XM_017011104.1:c.2858A>T	XP_016866593.1:p.Asn953Ile
XM_017011105.2:c.2858A>T	XP_016866594.1:p.Asn953Ile
XM_017011106.2:c.2858A>T	XP_016866595.1:p.Asn953Ile
XM_017011107.2:c.2678A>T	XP_016866596.1:p.Asn893Ile
XR_002956289.1:n.2941A>T
NM_001363725.2:c.527A>T	NP_001350654.1:p.Asn176Ile
NM_001371656.1:c.3065A>T	NP_001358585.1:p.Asn1022Ile
NM_001374820.1:c.3065A>T	NP_001361749.1:p.Asn1022Ile
NM_001374828.1:c.3026A>T MANE Select	NP_001361757.1:p.Asn1009Ile
NM_017519.3:c.3026A>T	NP_059989.3:p.Asn1009Ile