Canonical Allele Identifier: CA571644462

Gene: ARID1B

Linked Data

• dbSNP Id: rs1320696536
• gnomAD v2: 6-157469659-T-TACTC
• gnomAD v3: 6-157148525-T-TACTC
• gnomAD v4: 6-157148525-T-TACTC
• MyVariant Identifiers: chr6:g.157469659_157469660insACTC (hg19) ; chr6:g.157148525_157148526insACTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148526_157148529dup , CM000668.2:g.157148526_157148529dup	GRCh38
NC_000006.11:g.157469660_157469663dup , CM000668.1:g.157469660_157469663dup	GRCh37
NC_000006.10:g.157511352_157511355dup	NCBI36
NG_032093.1:g.375597_375600dup
NG_032093.2:g.375597_375600dup
NG_066624.1:g.377501_377504dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-98_2762-95dup	ENSP00000055163.8:n.2762-98_2762-95dup
ENST00000414678.8:c.2672-98_2672-95dup	ENSP00000412835.3:n.2672-98_2672-95dup
ENST00000637015.2:c.2762-98_2762-95dup	ENSP00000489729.2:n.2762-98_2762-95dup
ENST00000319584.11:c.776-98_776-95dup	ENSP00000313006.7:n.776-98_776-95dup
ENST00000346085.10:c.2801-98_2801-95dup	ENSP00000344546.5:n.2801-98_2801-95dup
ENST00000350026.10:c.2513-98_2513-95dup	ENSP00000055163.7:n.2513-98_2513-95dup
ENST00000414678.7:c.920-98_920-95dup	ENSP00000412835.2:n.920-98_920-95dup
ENST00000452544.2:n.663-98_663-95dup
ENST00000635849.1:c.83-98_83-95dup	ENSP00000490948.1:n.83-98_83-95dup
ENST00000636930.2:c.2762-98_2762-95dup MANE Select	ENSP00000490491.2:n.2762-98_2762-95dup
ENST00000637810.1:c.263-98_263-95dup	ENSP00000489636.1:n.263-98_263-95dup
ENST00000637904.1:c.263-98_263-95dup	ENSP00000490550.1:n.263-98_263-95dup
ENST00000647938.1:c.2552-98_2552-95dup	ENSP00000498155.1:n.2552-98_2552-95dup
ENST00000674190.1:n.1511-98_1511-95dup
ENST00000319584.10:c.779-98_779-95dup	ENSP00000313006.6:n.779-98_779-95dup
ENST00000346085.9:c.2552-98_2552-95dup	ENSP00000344546.4:n.2552-98_2552-95dup
ENST00000350026.9:c.2513-98_2513-95dup	ENSP00000055163.7:n.2513-98_2513-95dup
ENST00000414678.6:c.920-98_920-95dup	ENSP00000412835.2:n.920-98_920-95dup
ENST00000452544.1:n.609-98_609-95dup
NM_017519.2:c.2513-98_2513-95dup	NP_059989.2:n.2513-98_2513-95dup
NM_020732.3:c.2552-98_2552-95dup	NP_065783.3:n.2552-98_2552-95dup
XM_005267069.3:c.2513-98_2513-95dup	XP_005267126.2:n.2513-98_2513-95dup
XM_011535984.1:c.1463-98_1463-95dup	XP_011534286.1:n.1463-98_1463-95dup
XM_011535985.1:c.1283-98_1283-95dup	XP_011534287.1:n.1283-98_1283-95dup
XM_011535986.1:c.1043-98_1043-95dup	XP_011534288.1:n.1043-98_1043-95dup
XM_011535987.1:c.662-98_662-95dup	XP_011534289.1:n.662-98_662-95dup
XM_011535988.1:c.-20+15319_-20+15322dup	XP_011534290.1:n.-20+15319_-20+15322dup
NM_001346813.1:c.2513-98_2513-95dup	NP_001333742.1:n.2513-98_2513-95dup
NM_001363725.1:c.263-98_263-95dup	NP_001350654.1:n.263-98_263-95dup
XM_011535984.2:c.2594-98_2594-95dup	XP_011534286.2:n.2594-98_2594-95dup
XM_011535988.3:c.-20+15319_-20+15322dup	XP_011534290.1:n.-20+15319_-20+15322dup
XM_017011103.2:c.2594-98_2594-95dup	XP_016866592.1:n.2594-98_2594-95dup
XM_017011104.1:c.2594-98_2594-95dup	XP_016866593.1:n.2594-98_2594-95dup
XM_017011105.2:c.2594-98_2594-95dup	XP_016866594.1:n.2594-98_2594-95dup
XM_017011106.2:c.2594-98_2594-95dup	XP_016866595.1:n.2594-98_2594-95dup
XM_017011107.2:c.2414-98_2414-95dup	XP_016866596.1:n.2414-98_2414-95dup
XR_002956289.1:n.2677-98_2677-95dup
NM_001363725.2:c.263-98_263-95dup	NP_001350654.1:n.263-98_263-95dup
NM_001371656.1:c.2801-98_2801-95dup	NP_001358585.1:n.2801-98_2801-95dup
NM_001374820.1:c.2801-98_2801-95dup	NP_001361749.1:n.2801-98_2801-95dup
NM_001374828.1:c.2762-98_2762-95dup MANE Select	NP_001361757.1:n.2762-98_2762-95dup
NM_017519.3:c.2762-98_2762-95dup	NP_059989.3:n.2762-98_2762-95dup