Canonical Allele Identifier: CA2680917362

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148492-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148492G>A , CM000668.2:g.157148492G>A	GRCh38
NC_000006.11:g.157469626G>A , CM000668.1:g.157469626G>A	GRCh37
NC_000006.10:g.157511318G>A	NCBI36
NG_032093.1:g.375563G>A
NG_032093.2:g.375563G>A
NG_066624.1:g.377467G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-132G>A	ENSP00000055163.8:n.2762-132G>A
ENST00000414678.8:c.2672-132G>A	ENSP00000412835.3:n.2672-132G>A
ENST00000637015.2:c.2762-132G>A	ENSP00000489729.2:n.2762-132G>A
ENST00000319584.11:c.776-132G>A	ENSP00000313006.7:n.776-132G>A
ENST00000346085.10:c.2801-132G>A	ENSP00000344546.5:n.2801-132G>A
ENST00000350026.10:c.2513-132G>A	ENSP00000055163.7:n.2513-132G>A
ENST00000414678.7:c.920-132G>A	ENSP00000412835.2:n.920-132G>A
ENST00000452544.2:n.663-132G>A
ENST00000635849.1:c.83-132G>A	ENSP00000490948.1:n.83-132G>A
ENST00000636930.2:c.2762-132G>A MANE Select	ENSP00000490491.2:n.2762-132G>A
ENST00000637810.1:c.263-132G>A	ENSP00000489636.1:n.263-132G>A
ENST00000637904.1:c.263-132G>A	ENSP00000490550.1:n.263-132G>A
ENST00000647938.1:c.2552-132G>A	ENSP00000498155.1:n.2552-132G>A
ENST00000674190.1:n.1511-132G>A
ENST00000319584.10:c.779-132G>A	ENSP00000313006.6:n.779-132G>A
ENST00000346085.9:c.2552-132G>A	ENSP00000344546.4:n.2552-132G>A
ENST00000350026.9:c.2513-132G>A	ENSP00000055163.7:n.2513-132G>A
ENST00000414678.6:c.920-132G>A	ENSP00000412835.2:n.920-132G>A
ENST00000452544.1:n.609-132G>A
NM_017519.2:c.2513-132G>A	NP_059989.2:n.2513-132G>A
NM_020732.3:c.2552-132G>A	NP_065783.3:n.2552-132G>A
XM_005267069.3:c.2513-132G>A	XP_005267126.2:n.2513-132G>A
XM_011535984.1:c.1463-132G>A	XP_011534286.1:n.1463-132G>A
XM_011535985.1:c.1283-132G>A	XP_011534287.1:n.1283-132G>A
XM_011535986.1:c.1043-132G>A	XP_011534288.1:n.1043-132G>A
XM_011535987.1:c.662-132G>A	XP_011534289.1:n.662-132G>A
XM_011535988.1:c.-20+15285G>A	XP_011534290.1:n.-20+15285G>A
NM_001346813.1:c.2513-132G>A	NP_001333742.1:n.2513-132G>A
NM_001363725.1:c.263-132G>A	NP_001350654.1:n.263-132G>A
XM_011535984.2:c.2594-132G>A	XP_011534286.2:n.2594-132G>A
XM_011535988.3:c.-20+15285G>A	XP_011534290.1:n.-20+15285G>A
XM_017011103.2:c.2594-132G>A	XP_016866592.1:n.2594-132G>A
XM_017011104.1:c.2594-132G>A	XP_016866593.1:n.2594-132G>A
XM_017011105.2:c.2594-132G>A	XP_016866594.1:n.2594-132G>A
XM_017011106.2:c.2594-132G>A	XP_016866595.1:n.2594-132G>A
XM_017011107.2:c.2414-132G>A	XP_016866596.1:n.2414-132G>A
XR_002956289.1:n.2677-132G>A
NM_001363725.2:c.263-132G>A	NP_001350654.1:n.263-132G>A
NM_001371656.1:c.2801-132G>A	NP_001358585.1:n.2801-132G>A
NM_001374820.1:c.2801-132G>A	NP_001361749.1:n.2801-132G>A
NM_001374828.1:c.2762-132G>A MANE Select	NP_001361757.1:n.2762-132G>A
NM_017519.3:c.2762-132G>A	NP_059989.3:n.2762-132G>A