Canonical Allele Identifier: CA366388992

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469940A>T (hg19) ; chr6:g.157148806A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148806A>T , CM000668.2:g.157148806A>T	GRCh38
NC_000006.11:g.157469940A>T , CM000668.1:g.157469940A>T	GRCh37
NC_000006.10:g.157511632A>T	NCBI36
NG_032093.1:g.375877A>T
NG_032093.2:g.375877A>T
NG_066624.1:g.377781A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2944A>T	ENSP00000055163.8:p.Asn982Tyr
ENST00000414678.8:c.2854A>T	ENSP00000412835.3:p.Asn952Tyr
ENST00000637015.2:c.2944A>T	ENSP00000489729.2:p.Asn982Tyr
ENST00000319584.11:c.958A>T	ENSP00000313006.7:p.Asn320Tyr
ENST00000346085.10:c.2983A>T	ENSP00000344546.5:p.Asn995Tyr
ENST00000350026.10:c.2695A>T	ENSP00000055163.7:p.Asn899Tyr
ENST00000414678.7:c.1102A>T	ENSP00000412835.2:p.Asn368Tyr
ENST00000452544.2:n.845A>T
ENST00000635849.1:c.265A>T	ENSP00000490948.1:p.Asn89Tyr
ENST00000636426.1:n.78A>T
ENST00000636930.2:c.2944A>T MANE Select	ENSP00000490491.2:p.Asn982Tyr
ENST00000637015.1:c.183A>T
ENST00000637810.1:c.445A>T	ENSP00000489636.1:p.Asn149Tyr
ENST00000637904.1:c.445A>T	ENSP00000490550.1:p.Asn149Tyr
ENST00000647938.1:c.2734A>T	ENSP00000498155.1:p.Asn912Tyr
ENST00000674190.1:n.1693A>T
ENST00000319584.10:c.961A>T	ENSP00000313006.6:p.Asn321Tyr
ENST00000346085.9:c.2734A>T	ENSP00000344546.4:p.Asn912Tyr
ENST00000350026.9:c.2695A>T	ENSP00000055163.7:p.Asn899Tyr
ENST00000414678.6:c.1102A>T	ENSP00000412835.2:p.Asn368Tyr
ENST00000452544.1:n.791A>T
ENST00000478761.3:c.17A>T
NM_017519.2:c.2695A>T	NP_059989.2:p.Asn899Tyr
NM_020732.3:c.2734A>T	NP_065783.3:p.Asn912Tyr
XM_005267069.3:c.2695A>T	XP_005267126.2:p.Asn899Tyr
XM_011535984.1:c.1645A>T	XP_011534286.1:p.Asn549Tyr
XM_011535985.1:c.1465A>T	XP_011534287.1:p.Asn489Tyr
XM_011535986.1:c.1225A>T	XP_011534288.1:p.Asn409Tyr
XM_011535987.1:c.844A>T	XP_011534289.1:p.Asn282Tyr
XM_011535988.1:c.-20+15599A>T	XP_011534290.1:n.-20+15599A>T
NM_001346813.1:c.2695A>T	NP_001333742.1:p.Asn899Tyr
NM_001363725.1:c.445A>T	NP_001350654.1:p.Asn149Tyr
XM_011535984.2:c.2776A>T	XP_011534286.2:p.Asn926Tyr
XM_011535988.3:c.-20+15599A>T	XP_011534290.1:n.-20+15599A>T
XM_017011103.2:c.2776A>T	XP_016866592.1:p.Asn926Tyr
XM_017011104.1:c.2776A>T	XP_016866593.1:p.Asn926Tyr
XM_017011105.2:c.2776A>T	XP_016866594.1:p.Asn926Tyr
XM_017011106.2:c.2776A>T	XP_016866595.1:p.Asn926Tyr
XM_017011107.2:c.2596A>T	XP_016866596.1:p.Asn866Tyr
XR_002956289.1:n.2859A>T
NM_001363725.2:c.445A>T	NP_001350654.1:p.Asn149Tyr
NM_001371656.1:c.2983A>T	NP_001358585.1:p.Asn995Tyr
NM_001374820.1:c.2983A>T	NP_001361749.1:p.Asn995Tyr
NM_001374828.1:c.2944A>T MANE Select	NP_001361757.1:p.Asn982Tyr
NM_017519.3:c.2944A>T	NP_059989.3:p.Asn982Tyr