Canonical Allele Identifier: CA2680910654

Gene: ARID1B

Linked Data

• gnomAD v4: 6-156829207-CTTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829210_156829214del , CM000668.2:g.156829210_156829214del	GRCh38
NC_000006.11:g.157150344_157150348del , CM000668.1:g.157150344_157150348del	GRCh37
NC_000006.10:g.157192036_157192040del	NCBI36
NG_032093.1:g.56281_56285del
NG_032093.2:g.56281_56285del
NG_066624.1:g.58185_58189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1792-17_1792-13del	ENSP00000055163.8:n.1792-17_1792-13del
ENST00000414678.8:c.1792-17_1792-13del	ENSP00000412835.3:n.1792-17_1792-13del
ENST00000637015.2:c.1792-17_1792-13del	ENSP00000489729.2:n.1792-17_1792-13del
ENST00000346085.10:c.1792-17_1792-13del	ENSP00000344546.5:n.1792-17_1792-13del
ENST00000350026.10:c.1543-17_1543-13del	ENSP00000055163.7:n.1543-17_1543-13del
ENST00000414678.7:c.40-17_40-13del	ENSP00000412835.2:n.40-17_40-13del
ENST00000494260.2:c.73-17_73-13del	ENSP00000490094.1:n.73-17_73-13del
ENST00000636607.1:c.55-17_55-13del	ENSP00000490050.1:n.55-17_55-13del
ENST00000636748.1:c.73-17_73-13del	ENSP00000489917.1:n.73-17_73-13del
ENST00000636930.2:c.1792-17_1792-13del MANE Select	ENSP00000490491.2:n.1792-17_1792-13del
ENST00000637910.1:n.73-17_73-13del
ENST00000638000.1:c.9-17_9-13del
ENST00000647938.1:c.1543-17_1543-13del	ENSP00000498155.1:n.1543-17_1543-13del
ENST00000674190.1:n.499-17_499-13del
ENST00000674298.1:c.1532-17_1532-13del
ENST00000346085.9:c.1543-17_1543-13del	ENSP00000344546.4:n.1543-17_1543-13del
ENST00000350026.9:c.1543-17_1543-13del	ENSP00000055163.7:n.1543-17_1543-13del
ENST00000414678.6:c.40-17_40-13del	ENSP00000412835.2:n.40-17_40-13del
NM_017519.2:c.1543-17_1543-13del	NP_059989.2:n.1543-17_1543-13del
NM_020732.3:c.1543-17_1543-13del	NP_065783.3:n.1543-17_1543-13del
XM_005267069.3:c.1543-17_1543-13del	XP_005267126.2:n.1543-17_1543-13del
XM_011535984.1:c.412-17_412-13del	XP_011534286.1:n.412-17_412-13del
XM_011535985.1:c.412-17_412-13del	XP_011534287.1:n.412-17_412-13del
XM_011535986.1:c.-9-17_-9-13del	XP_011534288.1:n.-9-17_-9-13del
NM_001346813.1:c.1543-17_1543-13del	NP_001333742.1:n.1543-17_1543-13del
XM_011535984.2:c.1543-17_1543-13del	XP_011534286.2:n.1543-17_1543-13del
XM_017011103.2:c.1543-17_1543-13del	XP_016866592.1:n.1543-17_1543-13del
XM_017011104.1:c.1543-17_1543-13del	XP_016866593.1:n.1543-17_1543-13del
XM_017011105.2:c.1543-17_1543-13del	XP_016866594.1:n.1543-17_1543-13del
XM_017011106.2:c.1543-17_1543-13del	XP_016866595.1:n.1543-17_1543-13del
XM_017011107.2:c.1543-17_1543-13del	XP_016866596.1:n.1543-17_1543-13del
XR_002956289.1:n.1626-17_1626-13del
NM_001371656.1:c.1792-17_1792-13del	NP_001358585.1:n.1792-17_1792-13del
NM_001374820.1:c.1792-17_1792-13del	NP_001361749.1:n.1792-17_1792-13del
NM_001374828.1:c.1792-17_1792-13del MANE Select	NP_001361757.1:n.1792-17_1792-13del
NM_017519.3:c.1792-17_1792-13del	NP_059989.3:n.1792-17_1792-13del