Canonical Allele Identifier: CA366235306

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3979A>G	ENSP00000055163.8:p.Asn1327Asp
ENST00000414678.8:c.4048A>G	ENSP00000412835.3:p.Asn1350Asp
ENST00000637015.2:c.4267A>G	ENSP00000489729.2:p.Asn1423Asp
ENST00000346085.10:c.4018A>G	ENSP00000344546.5:p.Asn1340Asp
ENST00000350026.10:c.3730A>G	ENSP00000055163.7:p.Asn1244Asp
ENST00000414678.7:c.2296A>G	ENSP00000412835.2:p.Asn766Asp
ENST00000635849.1:c.1459A>G	ENSP00000490948.1:p.Asn487Asp
ENST00000635957.1:c.1090A>G	ENSP00000490385.1:p.Asn364Asp
ENST00000636930.2:c.4138A>G MANE Select	ENSP00000490491.2:p.Asn1380Asp
ENST00000636940.1:n.2135A>G
ENST00000637015.1:c.1506A>G
ENST00000637568.1:c.1420A>G
ENST00000637741.1:n.804A>G
ENST00000637810.1:c.1480A>G	ENSP00000489636.1:p.Asn494Asp
ENST00000637904.1:c.1639A>G	ENSP00000490550.1:p.Asn547Asp
ENST00000647938.1:c.3769A>G	ENSP00000498155.1:p.Asn1257Asp
ENST00000346085.9:c.3769A>G	ENSP00000344546.4:p.Asn1257Asp
ENST00000350026.9:c.3730A>G	ENSP00000055163.7:p.Asn1244Asp
ENST00000414678.6:c.2296A>G	ENSP00000412835.2:p.Asn766Asp
NM_017519.2:c.3730A>G	NP_059989.2:p.Asn1244Asp
NM_020732.3:c.3769A>G	NP_065783.3:p.Asn1257Asp
XM_005267069.3:c.3889A>G	XP_005267126.2:p.Asn1297Asp
XM_011535984.1:c.2968A>G	XP_011534286.1:p.Asn990Asp
XM_011535985.1:c.2788A>G	XP_011534287.1:p.Asn930Asp
XM_011535986.1:c.2548A>G	XP_011534288.1:p.Asn850Asp
XM_011535987.1:c.2167A>G	XP_011534289.1:p.Asn723Asp
XM_011535988.1:c.1030A>G	XP_011534290.1:p.Asn344Asp
NM_001346813.1:c.3889A>G	NP_001333742.1:p.Asn1297Asp
NM_001363725.1:c.1639A>G	NP_001350654.1:p.Asn547Asp
XM_011535984.2:c.4099A>G	XP_011534286.2:p.Asn1367Asp
XM_011535988.3:c.1030A>G	XP_011534290.1:p.Asn344Asp
XM_017011103.2:c.4000A>G	XP_016866592.1:p.Asn1334Asp
XM_017011104.1:c.3970A>G	XP_016866593.1:p.Asn1324Asp
XM_017011105.2:c.3940A>G	XP_016866594.1:p.Asn1314Asp
XM_017011106.2:c.3811A>G	XP_016866595.1:p.Asn1271Asp
XM_017011107.2:c.3790A>G	XP_016866596.1:p.Asn1264Asp
XR_002956289.1:n.4182A>G
NM_001363725.2:c.1639A>G	NP_001350654.1:p.Asn547Asp
NM_001371656.1:c.4018A>G	NP_001358585.1:p.Asn1340Asp
NM_001374820.1:c.4018A>G	NP_001361749.1:p.Asn1340Asp
NM_001374828.1:c.4138A>G MANE Select	NP_001361757.1:p.Asn1380Asp
NM_017519.3:c.3979A>G	NP_059989.3:p.Asn1327Asp