Canonical Allele Identifier: CA150838692

Gene: ARID1B

Linked Data

• dbSNP Id: rs974267163
• gnomAD v2: 6-157406018-A-G
• gnomAD v4: 6-157084884-A-G
• MyVariant Identifiers: chr6:g.157406018A>G (hg19) ; chr6:g.157084884A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084884A>G , CM000668.2:g.157084884A>G	GRCh38
NC_000006.11:g.157406018A>G , CM000668.1:g.157406018A>G	GRCh37
NC_000006.10:g.157447710A>G	NCBI36
NG_032093.1:g.311955A>G
NG_032093.2:g.311955A>G
NG_066624.1:g.313859A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2470A>G	ENSP00000055163.8:p.Ile824Val
ENST00000414678.8:c.2470A>G	ENSP00000412835.3:p.Ile824Val
ENST00000637015.2:c.2470A>G	ENSP00000489729.2:p.Ile824Val
ENST00000319584.11:c.484A>G	ENSP00000313006.7:p.Ile162Val
ENST00000346085.10:c.2509A>G	ENSP00000344546.5:p.Ile837Val
ENST00000350026.10:c.2221A>G	ENSP00000055163.7:p.Ile741Val
ENST00000414678.7:c.718A>G	ENSP00000412835.2:p.Ile240Val
ENST00000452544.2:n.371A>G
ENST00000493658.2:n.119A>G
ENST00000635849.1:c.-30A>G	ENSP00000490948.1:n.-30A>G
ENST00000636930.2:c.2470A>G MANE Select	ENSP00000490491.2:p.Ile824Val
ENST00000637003.1:c.-30A>G	ENSP00000489666.1:n.-30A>G
ENST00000637810.1:c.-30A>G	ENSP00000489636.1:n.-30A>G
ENST00000637904.1:c.-30A>G	ENSP00000490550.1:n.-30A>G
ENST00000647938.1:c.2260A>G	ENSP00000498155.1:p.Ile754Val
ENST00000674190.1:n.1219A>G
ENST00000319584.10:c.487A>G	ENSP00000313006.6:p.Ile163Val
ENST00000346085.9:c.2260A>G	ENSP00000344546.4:p.Ile754Val
ENST00000350026.9:c.2221A>G	ENSP00000055163.7:p.Ile741Val
ENST00000414678.6:c.718A>G	ENSP00000412835.2:p.Ile240Val
ENST00000452544.1:n.329A>G
ENST00000493658.1:n.119A>G
NM_017519.2:c.2221A>G	NP_059989.2:p.Ile741Val
NM_020732.3:c.2260A>G	NP_065783.3:p.Ile754Val
XM_005267069.3:c.2221A>G	XP_005267126.2:p.Ile741Val
XM_011535984.1:c.1171A>G	XP_011534286.1:p.Ile391Val
XM_011535985.1:c.1171A>G	XP_011534287.1:p.Ile391Val
XM_011535986.1:c.751A>G	XP_011534288.1:p.Ile251Val
XM_011535987.1:c.370A>G	XP_011534289.1:p.Ile124Val
NM_001346813.1:c.2221A>G	NP_001333742.1:p.Ile741Val
NM_001363725.1:c.-30A>G	NP_001350654.1:n.-30A>G
XM_011535984.2:c.2302A>G	XP_011534286.2:p.Ile768Val
XM_017011103.2:c.2302A>G	XP_016866592.1:p.Ile768Val
XM_017011104.1:c.2302A>G	XP_016866593.1:p.Ile768Val
XM_017011105.2:c.2302A>G	XP_016866594.1:p.Ile768Val
XM_017011106.2:c.2302A>G	XP_016866595.1:p.Ile768Val
XM_017011107.2:c.2302A>G	XP_016866596.1:p.Ile768Val
XR_002956289.1:n.2385A>G
NM_001363725.2:c.-30A>G	NP_001350654.1:n.-30A>G
NM_001371656.1:c.2509A>G	NP_001358585.1:p.Ile837Val
NM_001374820.1:c.2509A>G	NP_001361749.1:p.Ile837Val
NM_001374828.1:c.2470A>G MANE Select	NP_001361757.1:p.Ile824Val
NM_017519.3:c.2470A>G	NP_059989.3:p.Ile824Val