Canonical Allele Identifier: CA2680922142

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181221-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181222del , CM000668.2:g.157181222del	GRCh38
NC_000006.11:g.157502356del , CM000668.1:g.157502356del	GRCh37
NC_000006.10:g.157544048del	NCBI36
NG_032093.1:g.408293del
NG_032093.2:g.408293del
NG_066624.1:g.410197del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3555+44del	ENSP00000055163.8:n.3555+44del
ENST00000414678.8:c.3624+44del	ENSP00000412835.3:n.3624+44del
ENST00000637015.2:c.3843+44del	ENSP00000489729.2:n.3843+44del
ENST00000319584.11:c.1728+44del	ENSP00000313006.7:n.1728+44del
ENST00000346085.10:c.3594+44del	ENSP00000344546.5:n.3594+44del
ENST00000350026.10:c.3306+44del	ENSP00000055163.7:n.3306+44del
ENST00000414678.7:c.1872+44del	ENSP00000412835.2:n.1872+44del
ENST00000635849.1:c.1035+44del	ENSP00000490948.1:n.1035+44del
ENST00000635957.1:c.669+44del	ENSP00000490385.1:n.669+44del
ENST00000636930.2:c.3714+44del MANE Select	ENSP00000490491.2:n.3714+44del
ENST00000636940.1:n.1711+44del
ENST00000637015.1:c.1082+44del
ENST00000637568.1:c.996+44del
ENST00000637741.1:n.380+44del
ENST00000637810.1:c.1056+44del	ENSP00000489636.1:n.1056+44del
ENST00000637904.1:c.1215+44del	ENSP00000490550.1:n.1215+44del
ENST00000647938.1:c.3345+44del	ENSP00000498155.1:n.3345+44del
ENST00000319584.10:c.1731+44del	ENSP00000313006.6:n.1731+44del
ENST00000346085.9:c.3345+44del	ENSP00000344546.4:n.3345+44del
ENST00000350026.9:c.3306+44del	ENSP00000055163.7:n.3306+44del
ENST00000400790.3:c.507+44del	ENSP00000383596.3:n.507+44del
ENST00000414678.6:c.1872+44del	ENSP00000412835.2:n.1872+44del
NM_017519.2:c.3306+44del	NP_059989.2:n.3306+44del
NM_020732.3:c.3345+44del	NP_065783.3:n.3345+44del
XM_005267069.3:c.3465+44del	XP_005267126.2:n.3465+44del
XM_011535984.1:c.2544+44del	XP_011534286.1:n.2544+44del
XM_011535985.1:c.2364+44del	XP_011534287.1:n.2364+44del
XM_011535986.1:c.2124+44del	XP_011534288.1:n.2124+44del
XM_011535987.1:c.1743+44del	XP_011534289.1:n.1743+44del
XM_011535988.1:c.606+44del	XP_011534290.1:n.606+44del
NM_001346813.1:c.3465+44del	NP_001333742.1:n.3465+44del
NM_001363725.1:c.1215+44del	NP_001350654.1:n.1215+44del
XM_011535984.2:c.3675+44del	XP_011534286.2:n.3675+44del
XM_011535988.3:c.606+44del	XP_011534290.1:n.606+44del
XM_017011103.2:c.3576+44del	XP_016866592.1:n.3576+44del
XM_017011104.1:c.3546+44del	XP_016866593.1:n.3546+44del
XM_017011105.2:c.3516+44del	XP_016866594.1:n.3516+44del
XM_017011106.2:c.3387+44del	XP_016866595.1:n.3387+44del
XM_017011107.2:c.3366+44del	XP_016866596.1:n.3366+44del
XR_002956289.1:n.3758+44del
NM_001363725.2:c.1215+44del	NP_001350654.1:n.1215+44del
NM_001371656.1:c.3594+44del	NP_001358585.1:n.3594+44del
NM_001374820.1:c.3594+44del	NP_001361749.1:n.3594+44del
NM_001374828.1:c.3714+44del MANE Select	NP_001361757.1:n.3714+44del
NM_017519.3:c.3555+44del	NP_059989.3:n.3555+44del