Canonical Allele Identifier: CA4067368

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2054974
• ClinVar RCV Id: RCV002909922
• dbSNP Id: rs374705142
• ExAC: 6:157502255 G / A
• gnomAD v2: 6-157502255-G-A
• gnomAD v3: 6-157181121-G-A
• gnomAD v4: 6-157181121-G-A
• MyVariant Identifiers: chr6:g.157502255G>A (hg19) ; chr6:g.157181121G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181121G>A , CM000668.2:g.157181121G>A	GRCh38
NC_000006.11:g.157502255G>A , CM000668.1:g.157502255G>A	GRCh37
NC_000006.10:g.157543947G>A	NCBI36
NG_032093.1:g.408192G>A
NG_032093.2:g.408192G>A
NG_066624.1:g.410096G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3498G>A	ENSP00000055163.8:p.Lys1166=
ENST00000414678.8:c.3567G>A	ENSP00000412835.3:p.Lys1189=
ENST00000637015.2:c.3786G>A	ENSP00000489729.2:p.Lys1262=
ENST00000319584.11:c.1671G>A	ENSP00000313006.7:p.Lys557=
ENST00000346085.10:c.3537G>A	ENSP00000344546.5:p.Lys1179=
ENST00000350026.10:c.3249G>A	ENSP00000055163.7:p.Lys1083=
ENST00000414678.7:c.1815G>A	ENSP00000412835.2:p.Lys605=
ENST00000635849.1:c.978G>A	ENSP00000490948.1:p.Lys326=
ENST00000635957.1:c.612G>A	ENSP00000490385.1:p.Lys204=
ENST00000636930.2:c.3657G>A MANE Select	ENSP00000490491.2:p.Lys1219=
ENST00000636940.1:n.1654G>A
ENST00000637015.1:c.1025G>A
ENST00000637568.1:c.939G>A
ENST00000637741.1:n.323G>A
ENST00000637810.1:c.999G>A	ENSP00000489636.1:p.Lys333=
ENST00000637904.1:c.1158G>A	ENSP00000490550.1:p.Lys386=
ENST00000647938.1:c.3288G>A	ENSP00000498155.1:p.Lys1096=
ENST00000319584.10:c.1674G>A	ENSP00000313006.6:p.Lys558=
ENST00000346085.9:c.3288G>A	ENSP00000344546.4:p.Lys1096=
ENST00000350026.9:c.3249G>A	ENSP00000055163.7:p.Lys1083=
ENST00000400790.3:c.450G>A	ENSP00000383596.3:p.Lys150=
ENST00000414678.6:c.1815G>A	ENSP00000412835.2:p.Lys605=
ENST00000478761.3:c.859G>A
NM_017519.2:c.3249G>A	NP_059989.2:p.Lys1083=
NM_020732.3:c.3288G>A	NP_065783.3:p.Lys1096=
XM_005267069.3:c.3408G>A	XP_005267126.2:p.Lys1136=
XM_011535984.1:c.2487G>A	XP_011534286.1:p.Lys829=
XM_011535985.1:c.2307G>A	XP_011534287.1:p.Lys769=
XM_011535986.1:c.2067G>A	XP_011534288.1:p.Lys689=
XM_011535987.1:c.1686G>A	XP_011534289.1:p.Lys562=
XM_011535988.1:c.549G>A	XP_011534290.1:p.Lys183=
NM_001346813.1:c.3408G>A	NP_001333742.1:p.Lys1136=
NM_001363725.1:c.1158G>A	NP_001350654.1:p.Lys386=
XM_011535984.2:c.3618G>A	XP_011534286.2:p.Lys1206=
XM_011535988.3:c.549G>A	XP_011534290.1:p.Lys183=
XM_017011103.2:c.3519G>A	XP_016866592.1:p.Lys1173=
XM_017011104.1:c.3489G>A	XP_016866593.1:p.Lys1163=
XM_017011105.2:c.3459G>A	XP_016866594.1:p.Lys1153=
XM_017011106.2:c.3330G>A	XP_016866595.1:p.Lys1110=
XM_017011107.2:c.3309G>A	XP_016866596.1:p.Lys1103=
XR_002956289.1:n.3701G>A
NM_001363725.2:c.1158G>A	NP_001350654.1:p.Lys386=
NM_001371656.1:c.3537G>A	NP_001358585.1:p.Lys1179=
NM_001374820.1:c.3537G>A	NP_001361749.1:p.Lys1179=
NM_001374828.1:c.3657G>A MANE Select	NP_001361757.1:p.Lys1219=
NM_017519.3:c.3498G>A	NP_059989.3:p.Lys1166=