Canonical Allele Identifier: CA366227359

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316898
• MyVariant Identifiers: chr6:g.157502160A>G (hg19) ; chr6:g.157181026A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181026A>G , CM000668.2:g.157181026A>G	GRCh38
NC_000006.11:g.157502160A>G , CM000668.1:g.157502160A>G	GRCh37
NC_000006.10:g.157543852A>G	NCBI36
NG_032093.1:g.408097A>G
NG_032093.2:g.408097A>G
NG_066624.1:g.410001A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3403A>G	ENSP00000055163.8:p.Asn1135Asp
ENST00000414678.8:c.3472A>G	ENSP00000412835.3:p.Asn1158Asp
ENST00000637015.2:c.3691A>G	ENSP00000489729.2:p.Asn1231Asp
ENST00000319584.11:c.1576A>G	ENSP00000313006.7:p.Asn526Asp
ENST00000346085.10:c.3442A>G	ENSP00000344546.5:p.Asn1148Asp
ENST00000350026.10:c.3154A>G	ENSP00000055163.7:p.Asn1052Asp
ENST00000414678.7:c.1720A>G	ENSP00000412835.2:p.Asn574Asp
ENST00000635849.1:c.883A>G	ENSP00000490948.1:p.Asn295Asp
ENST00000635957.1:c.517A>G	ENSP00000490385.1:p.Asn173Asp
ENST00000636930.2:c.3562A>G MANE Select	ENSP00000490491.2:p.Asn1188Asp
ENST00000636940.1:n.1559A>G
ENST00000637015.1:c.930A>G
ENST00000637568.1:c.844A>G
ENST00000637741.1:n.228A>G
ENST00000637810.1:c.904A>G	ENSP00000489636.1:p.Asn302Asp
ENST00000637904.1:c.1063A>G	ENSP00000490550.1:p.Asn355Asp
ENST00000647938.1:c.3193A>G	ENSP00000498155.1:p.Asn1065Asp
ENST00000319584.10:c.1579A>G	ENSP00000313006.6:p.Asn527Asp
ENST00000346085.9:c.3193A>G	ENSP00000344546.4:p.Asn1065Asp
ENST00000350026.9:c.3154A>G	ENSP00000055163.7:p.Asn1052Asp
ENST00000400790.3:c.355A>G	ENSP00000383596.3:p.Asn119Asp
ENST00000414678.6:c.1720A>G	ENSP00000412835.2:p.Asn574Asp
ENST00000478761.3:c.764A>G
NM_017519.2:c.3154A>G	NP_059989.2:p.Asn1052Asp
NM_020732.3:c.3193A>G	NP_065783.3:p.Asn1065Asp
XM_005267069.3:c.3313A>G	XP_005267126.2:p.Asn1105Asp
XM_011535984.1:c.2392A>G	XP_011534286.1:p.Asn798Asp
XM_011535985.1:c.2212A>G	XP_011534287.1:p.Asn738Asp
XM_011535986.1:c.1972A>G	XP_011534288.1:p.Asn658Asp
XM_011535987.1:c.1591A>G	XP_011534289.1:p.Asn531Asp
XM_011535988.1:c.454A>G	XP_011534290.1:p.Asn152Asp
NM_001346813.1:c.3313A>G	NP_001333742.1:p.Asn1105Asp
NM_001363725.1:c.1063A>G	NP_001350654.1:p.Asn355Asp
XM_011535984.2:c.3523A>G	XP_011534286.2:p.Asn1175Asp
XM_011535988.3:c.454A>G	XP_011534290.1:p.Asn152Asp
XM_017011103.2:c.3424A>G	XP_016866592.1:p.Asn1142Asp
XM_017011104.1:c.3394A>G	XP_016866593.1:p.Asn1132Asp
XM_017011105.2:c.3364A>G	XP_016866594.1:p.Asn1122Asp
XM_017011106.2:c.3235A>G	XP_016866595.1:p.Asn1079Asp
XM_017011107.2:c.3214A>G	XP_016866596.1:p.Asn1072Asp
XR_002956289.1:n.3606A>G
NM_001363725.2:c.1063A>G	NP_001350654.1:p.Asn355Asp
NM_001371656.1:c.3442A>G	NP_001358585.1:p.Asn1148Asp
NM_001374820.1:c.3442A>G	NP_001361749.1:p.Asn1148Asp
NM_001374828.1:c.3562A>G MANE Select	NP_001361757.1:p.Asn1188Asp
NM_017519.3:c.3403A>G	NP_059989.3:p.Asn1135Asp