Canonical Allele Identifier: CA366389201

Gene: ARID1B

Linked Data

• dbSNP Id: rs1789996516
• gnomAD v3: 6-157148900-A-G
• gnomAD v4: 6-157148900-A-G
• MyVariant Identifiers: chr6:g.157470034A>G (hg19) ; chr6:g.157148900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148900A>G , CM000668.2:g.157148900A>G	GRCh38
NC_000006.11:g.157470034A>G , CM000668.1:g.157470034A>G	GRCh37
NC_000006.10:g.157511726A>G	NCBI36
NG_032093.1:g.375971A>G
NG_032093.2:g.375971A>G
NG_066624.1:g.377875A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3038A>G	ENSP00000055163.8:p.Gln1013Arg
ENST00000414678.8:c.2948A>G	ENSP00000412835.3:p.Gln983Arg
ENST00000637015.2:c.3038A>G	ENSP00000489729.2:p.Gln1013Arg
ENST00000319584.11:c.1052A>G	ENSP00000313006.7:p.Gln351Arg
ENST00000346085.10:c.3077A>G	ENSP00000344546.5:p.Gln1026Arg
ENST00000350026.10:c.2789A>G	ENSP00000055163.7:p.Gln930Arg
ENST00000414678.7:c.1196A>G	ENSP00000412835.2:p.Gln399Arg
ENST00000452544.2:n.939A>G
ENST00000635849.1:c.359A>G	ENSP00000490948.1:p.Gln120Arg
ENST00000636426.1:n.172A>G
ENST00000636930.2:c.3038A>G MANE Select	ENSP00000490491.2:p.Gln1013Arg
ENST00000637015.1:c.277A>G
ENST00000637568.1:c.81A>G
ENST00000637810.1:c.539A>G	ENSP00000489636.1:p.Gln180Arg
ENST00000637904.1:c.539A>G	ENSP00000490550.1:p.Gln180Arg
ENST00000647938.1:c.2828A>G	ENSP00000498155.1:p.Gln943Arg
ENST00000674190.1:n.1787A>G
ENST00000319584.10:c.1055A>G	ENSP00000313006.6:p.Gln352Arg
ENST00000346085.9:c.2828A>G	ENSP00000344546.4:p.Gln943Arg
ENST00000350026.9:c.2789A>G	ENSP00000055163.7:p.Gln930Arg
ENST00000414678.6:c.1196A>G	ENSP00000412835.2:p.Gln399Arg
ENST00000452544.1:n.885A>G
ENST00000478761.3:c.111A>G
NM_017519.2:c.2789A>G	NP_059989.2:p.Gln930Arg
NM_020732.3:c.2828A>G	NP_065783.3:p.Gln943Arg
XM_005267069.3:c.2789A>G	XP_005267126.2:p.Gln930Arg
XM_011535984.1:c.1739A>G	XP_011534286.1:p.Gln580Arg
XM_011535985.1:c.1559A>G	XP_011534287.1:p.Gln520Arg
XM_011535986.1:c.1319A>G	XP_011534288.1:p.Gln440Arg
XM_011535987.1:c.938A>G	XP_011534289.1:p.Gln313Arg
XM_011535988.1:c.-20+15693A>G	XP_011534290.1:n.-20+15693A>G
NM_001346813.1:c.2789A>G	NP_001333742.1:p.Gln930Arg
NM_001363725.1:c.539A>G	NP_001350654.1:p.Gln180Arg
XM_011535984.2:c.2870A>G	XP_011534286.2:p.Gln957Arg
XM_011535988.3:c.-20+15693A>G	XP_011534290.1:n.-20+15693A>G
XM_017011103.2:c.2870A>G	XP_016866592.1:p.Gln957Arg
XM_017011104.1:c.2870A>G	XP_016866593.1:p.Gln957Arg
XM_017011105.2:c.2870A>G	XP_016866594.1:p.Gln957Arg
XM_017011106.2:c.2870A>G	XP_016866595.1:p.Gln957Arg
XM_017011107.2:c.2690A>G	XP_016866596.1:p.Gln897Arg
XR_002956289.1:n.2953A>G
NM_001363725.2:c.539A>G	NP_001350654.1:p.Gln180Arg
NM_001371656.1:c.3077A>G	NP_001358585.1:p.Gln1026Arg
NM_001374820.1:c.3077A>G	NP_001361749.1:p.Gln1026Arg
NM_001374828.1:c.3038A>G MANE Select	NP_001361757.1:p.Gln1013Arg
NM_017519.3:c.3038A>G	NP_059989.3:p.Gln1013Arg