Canonical Allele Identifier: CA366235304

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339754
• MyVariant Identifiers: chr6:g.157511251A>C (hg19) ; chr6:g.157190117A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190117A>C , CM000668.2:g.157190117A>C	GRCh38
NC_000006.11:g.157511251A>C , CM000668.1:g.157511251A>C	GRCh37
NC_000006.10:g.157552943A>C	NCBI36
NG_032093.1:g.417188A>C
NG_032093.2:g.417188A>C
NG_066624.1:g.419092A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3979A>C	ENSP00000055163.8:p.Asn1327His
ENST00000414678.8:c.4048A>C	ENSP00000412835.3:p.Asn1350His
ENST00000637015.2:c.4267A>C	ENSP00000489729.2:p.Asn1423His
ENST00000346085.10:c.4018A>C	ENSP00000344546.5:p.Asn1340His
ENST00000350026.10:c.3730A>C	ENSP00000055163.7:p.Asn1244His
ENST00000414678.7:c.2296A>C	ENSP00000412835.2:p.Asn766His
ENST00000635849.1:c.1459A>C	ENSP00000490948.1:p.Asn487His
ENST00000635957.1:c.1090A>C	ENSP00000490385.1:p.Asn364His
ENST00000636930.2:c.4138A>C MANE Select	ENSP00000490491.2:p.Asn1380His
ENST00000636940.1:n.2135A>C
ENST00000637015.1:c.1506A>C
ENST00000637568.1:c.1420A>C
ENST00000637741.1:n.804A>C
ENST00000637810.1:c.1480A>C	ENSP00000489636.1:p.Asn494His
ENST00000637904.1:c.1639A>C	ENSP00000490550.1:p.Asn547His
ENST00000647938.1:c.3769A>C	ENSP00000498155.1:p.Asn1257His
ENST00000346085.9:c.3769A>C	ENSP00000344546.4:p.Asn1257His
ENST00000350026.9:c.3730A>C	ENSP00000055163.7:p.Asn1244His
ENST00000414678.6:c.2296A>C	ENSP00000412835.2:p.Asn766His
NM_017519.2:c.3730A>C	NP_059989.2:p.Asn1244His
NM_020732.3:c.3769A>C	NP_065783.3:p.Asn1257His
XM_005267069.3:c.3889A>C	XP_005267126.2:p.Asn1297His
XM_011535984.1:c.2968A>C	XP_011534286.1:p.Asn990His
XM_011535985.1:c.2788A>C	XP_011534287.1:p.Asn930His
XM_011535986.1:c.2548A>C	XP_011534288.1:p.Asn850His
XM_011535987.1:c.2167A>C	XP_011534289.1:p.Asn723His
XM_011535988.1:c.1030A>C	XP_011534290.1:p.Asn344His
NM_001346813.1:c.3889A>C	NP_001333742.1:p.Asn1297His
NM_001363725.1:c.1639A>C	NP_001350654.1:p.Asn547His
XM_011535984.2:c.4099A>C	XP_011534286.2:p.Asn1367His
XM_011535988.3:c.1030A>C	XP_011534290.1:p.Asn344His
XM_017011103.2:c.4000A>C	XP_016866592.1:p.Asn1334His
XM_017011104.1:c.3970A>C	XP_016866593.1:p.Asn1324His
XM_017011105.2:c.3940A>C	XP_016866594.1:p.Asn1314His
XM_017011106.2:c.3811A>C	XP_016866595.1:p.Asn1271His
XM_017011107.2:c.3790A>C	XP_016866596.1:p.Asn1264His
XR_002956289.1:n.4182A>C
NM_001363725.2:c.1639A>C	NP_001350654.1:p.Asn547His
NM_001371656.1:c.4018A>C	NP_001358585.1:p.Asn1340His
NM_001374820.1:c.4018A>C	NP_001361749.1:p.Asn1340His
NM_001374828.1:c.4138A>C MANE Select	NP_001361757.1:p.Asn1380His
NM_017519.3:c.3979A>C	NP_059989.3:p.Asn1327His