Canonical Allele Identifier: CA150846245

Gene: ARID1B

Linked Data

• dbSNP Id: rs541721882
• gnomAD v3: 6-157148562-T-A
• gnomAD v4: 6-157148562-T-A
• MyVariant Identifiers: chr6:g.157469696T>A (hg19) ; chr6:g.157148562T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148562T>A , CM000668.2:g.157148562T>A	GRCh38
NC_000006.11:g.157469696T>A , CM000668.1:g.157469696T>A	GRCh37
NC_000006.10:g.157511388T>A	NCBI36
NG_032093.1:g.375633T>A
NG_032093.2:g.375633T>A
NG_066624.1:g.377537T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-62T>A	ENSP00000055163.8:n.2762-62T>A
ENST00000414678.8:c.2672-62T>A	ENSP00000412835.3:n.2672-62T>A
ENST00000637015.2:c.2762-62T>A	ENSP00000489729.2:n.2762-62T>A
ENST00000319584.11:c.776-62T>A	ENSP00000313006.7:n.776-62T>A
ENST00000346085.10:c.2801-62T>A	ENSP00000344546.5:n.2801-62T>A
ENST00000350026.10:c.2513-62T>A	ENSP00000055163.7:n.2513-62T>A
ENST00000414678.7:c.920-62T>A	ENSP00000412835.2:n.920-62T>A
ENST00000452544.2:n.663-62T>A
ENST00000635849.1:c.83-62T>A	ENSP00000490948.1:n.83-62T>A
ENST00000636930.2:c.2762-62T>A MANE Select	ENSP00000490491.2:n.2762-62T>A
ENST00000637810.1:c.263-62T>A	ENSP00000489636.1:n.263-62T>A
ENST00000637904.1:c.263-62T>A	ENSP00000490550.1:n.263-62T>A
ENST00000647938.1:c.2552-62T>A	ENSP00000498155.1:n.2552-62T>A
ENST00000674190.1:n.1511-62T>A
ENST00000319584.10:c.779-62T>A	ENSP00000313006.6:n.779-62T>A
ENST00000346085.9:c.2552-62T>A	ENSP00000344546.4:n.2552-62T>A
ENST00000350026.9:c.2513-62T>A	ENSP00000055163.7:n.2513-62T>A
ENST00000414678.6:c.920-62T>A	ENSP00000412835.2:n.920-62T>A
ENST00000452544.1:n.609-62T>A
NM_017519.2:c.2513-62T>A	NP_059989.2:n.2513-62T>A
NM_020732.3:c.2552-62T>A	NP_065783.3:n.2552-62T>A
XM_005267069.3:c.2513-62T>A	XP_005267126.2:n.2513-62T>A
XM_011535984.1:c.1463-62T>A	XP_011534286.1:n.1463-62T>A
XM_011535985.1:c.1283-62T>A	XP_011534287.1:n.1283-62T>A
XM_011535986.1:c.1043-62T>A	XP_011534288.1:n.1043-62T>A
XM_011535987.1:c.662-62T>A	XP_011534289.1:n.662-62T>A
XM_011535988.1:c.-20+15355T>A	XP_011534290.1:n.-20+15355T>A
NM_001346813.1:c.2513-62T>A	NP_001333742.1:n.2513-62T>A
NM_001363725.1:c.263-62T>A	NP_001350654.1:n.263-62T>A
XM_011535984.2:c.2594-62T>A	XP_011534286.2:n.2594-62T>A
XM_011535988.3:c.-20+15355T>A	XP_011534290.1:n.-20+15355T>A
XM_017011103.2:c.2594-62T>A	XP_016866592.1:n.2594-62T>A
XM_017011104.1:c.2594-62T>A	XP_016866593.1:n.2594-62T>A
XM_017011105.2:c.2594-62T>A	XP_016866594.1:n.2594-62T>A
XM_017011106.2:c.2594-62T>A	XP_016866595.1:n.2594-62T>A
XM_017011107.2:c.2414-62T>A	XP_016866596.1:n.2414-62T>A
XR_002956289.1:n.2677-62T>A
NM_001363725.2:c.263-62T>A	NP_001350654.1:n.263-62T>A
NM_001371656.1:c.2801-62T>A	NP_001358585.1:n.2801-62T>A
NM_001374820.1:c.2801-62T>A	NP_001361749.1:n.2801-62T>A
NM_001374828.1:c.2762-62T>A MANE Select	NP_001361757.1:n.2762-62T>A
NM_017519.3:c.2762-62T>A	NP_059989.3:n.2762-62T>A