Canonical Allele Identifier: CA366388991

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2944A>C	ENSP00000055163.8:p.Asn982His
ENST00000414678.8:c.2854A>C	ENSP00000412835.3:p.Asn952His
ENST00000637015.2:c.2944A>C	ENSP00000489729.2:p.Asn982His
ENST00000319584.11:c.958A>C	ENSP00000313006.7:p.Asn320His
ENST00000346085.10:c.2983A>C	ENSP00000344546.5:p.Asn995His
ENST00000350026.10:c.2695A>C	ENSP00000055163.7:p.Asn899His
ENST00000414678.7:c.1102A>C	ENSP00000412835.2:p.Asn368His
ENST00000452544.2:n.845A>C
ENST00000635849.1:c.265A>C	ENSP00000490948.1:p.Asn89His
ENST00000636426.1:n.78A>C
ENST00000636930.2:c.2944A>C MANE Select	ENSP00000490491.2:p.Asn982His
ENST00000637015.1:c.183A>C
ENST00000637810.1:c.445A>C	ENSP00000489636.1:p.Asn149His
ENST00000637904.1:c.445A>C	ENSP00000490550.1:p.Asn149His
ENST00000647938.1:c.2734A>C	ENSP00000498155.1:p.Asn912His
ENST00000674190.1:n.1693A>C
ENST00000319584.10:c.961A>C	ENSP00000313006.6:p.Asn321His
ENST00000346085.9:c.2734A>C	ENSP00000344546.4:p.Asn912His
ENST00000350026.9:c.2695A>C	ENSP00000055163.7:p.Asn899His
ENST00000414678.6:c.1102A>C	ENSP00000412835.2:p.Asn368His
ENST00000452544.1:n.791A>C
ENST00000478761.3:c.17A>C
NM_017519.2:c.2695A>C	NP_059989.2:p.Asn899His
NM_020732.3:c.2734A>C	NP_065783.3:p.Asn912His
XM_005267069.3:c.2695A>C	XP_005267126.2:p.Asn899His
XM_011535984.1:c.1645A>C	XP_011534286.1:p.Asn549His
XM_011535985.1:c.1465A>C	XP_011534287.1:p.Asn489His
XM_011535986.1:c.1225A>C	XP_011534288.1:p.Asn409His
XM_011535987.1:c.844A>C	XP_011534289.1:p.Asn282His
XM_011535988.1:c.-20+15599A>C	XP_011534290.1:n.-20+15599A>C
NM_001346813.1:c.2695A>C	NP_001333742.1:p.Asn899His
NM_001363725.1:c.445A>C	NP_001350654.1:p.Asn149His
XM_011535984.2:c.2776A>C	XP_011534286.2:p.Asn926His
XM_011535988.3:c.-20+15599A>C	XP_011534290.1:n.-20+15599A>C
XM_017011103.2:c.2776A>C	XP_016866592.1:p.Asn926His
XM_017011104.1:c.2776A>C	XP_016866593.1:p.Asn926His
XM_017011105.2:c.2776A>C	XP_016866594.1:p.Asn926His
XM_017011106.2:c.2776A>C	XP_016866595.1:p.Asn926His
XM_017011107.2:c.2596A>C	XP_016866596.1:p.Asn866His
XR_002956289.1:n.2859A>C
NM_001363725.2:c.445A>C	NP_001350654.1:p.Asn149His
NM_001371656.1:c.2983A>C	NP_001358585.1:p.Asn995His
NM_001374820.1:c.2983A>C	NP_001361749.1:p.Asn995His
NM_001374828.1:c.2944A>C MANE Select	NP_001361757.1:p.Asn982His
NM_017519.3:c.2944A>C	NP_059989.3:p.Asn982His