Canonical Allele Identifier: CA366227362

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181026-A-T
• MyVariant Identifiers: chr6:g.157502160A>T (hg19) ; chr6:g.157181026A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3403A>T	ENSP00000055163.8:p.Asn1135Tyr
ENST00000414678.8:c.3472A>T	ENSP00000412835.3:p.Asn1158Tyr
ENST00000637015.2:c.3691A>T	ENSP00000489729.2:p.Asn1231Tyr
ENST00000319584.11:c.1576A>T	ENSP00000313006.7:p.Asn526Tyr
ENST00000346085.10:c.3442A>T	ENSP00000344546.5:p.Asn1148Tyr
ENST00000350026.10:c.3154A>T	ENSP00000055163.7:p.Asn1052Tyr
ENST00000414678.7:c.1720A>T	ENSP00000412835.2:p.Asn574Tyr
ENST00000635849.1:c.883A>T	ENSP00000490948.1:p.Asn295Tyr
ENST00000635957.1:c.517A>T	ENSP00000490385.1:p.Asn173Tyr
ENST00000636930.2:c.3562A>T MANE Select	ENSP00000490491.2:p.Asn1188Tyr
ENST00000636940.1:n.1559A>T
ENST00000637015.1:c.930A>T
ENST00000637568.1:c.844A>T
ENST00000637741.1:n.228A>T
ENST00000637810.1:c.904A>T	ENSP00000489636.1:p.Asn302Tyr
ENST00000637904.1:c.1063A>T	ENSP00000490550.1:p.Asn355Tyr
ENST00000647938.1:c.3193A>T	ENSP00000498155.1:p.Asn1065Tyr
ENST00000319584.10:c.1579A>T	ENSP00000313006.6:p.Asn527Tyr
ENST00000346085.9:c.3193A>T	ENSP00000344546.4:p.Asn1065Tyr
ENST00000350026.9:c.3154A>T	ENSP00000055163.7:p.Asn1052Tyr
ENST00000400790.3:c.355A>T	ENSP00000383596.3:p.Asn119Tyr
ENST00000414678.6:c.1720A>T	ENSP00000412835.2:p.Asn574Tyr
ENST00000478761.3:c.764A>T
NM_017519.2:c.3154A>T	NP_059989.2:p.Asn1052Tyr
NM_020732.3:c.3193A>T	NP_065783.3:p.Asn1065Tyr
XM_005267069.3:c.3313A>T	XP_005267126.2:p.Asn1105Tyr
XM_011535984.1:c.2392A>T	XP_011534286.1:p.Asn798Tyr
XM_011535985.1:c.2212A>T	XP_011534287.1:p.Asn738Tyr
XM_011535986.1:c.1972A>T	XP_011534288.1:p.Asn658Tyr
XM_011535987.1:c.1591A>T	XP_011534289.1:p.Asn531Tyr
XM_011535988.1:c.454A>T	XP_011534290.1:p.Asn152Tyr
NM_001346813.1:c.3313A>T	NP_001333742.1:p.Asn1105Tyr
NM_001363725.1:c.1063A>T	NP_001350654.1:p.Asn355Tyr
XM_011535984.2:c.3523A>T	XP_011534286.2:p.Asn1175Tyr
XM_011535988.3:c.454A>T	XP_011534290.1:p.Asn152Tyr
XM_017011103.2:c.3424A>T	XP_016866592.1:p.Asn1142Tyr
XM_017011104.1:c.3394A>T	XP_016866593.1:p.Asn1132Tyr
XM_017011105.2:c.3364A>T	XP_016866594.1:p.Asn1122Tyr
XM_017011106.2:c.3235A>T	XP_016866595.1:p.Asn1079Tyr
XM_017011107.2:c.3214A>T	XP_016866596.1:p.Asn1072Tyr
XR_002956289.1:n.3606A>T
NM_001363725.2:c.1063A>T	NP_001350654.1:p.Asn355Tyr
NM_001371656.1:c.3442A>T	NP_001358585.1:p.Asn1148Tyr
NM_001374820.1:c.3442A>T	NP_001361749.1:p.Asn1148Tyr
NM_001374828.1:c.3562A>T MANE Select	NP_001361757.1:p.Asn1188Tyr
NM_017519.3:c.3403A>T	NP_059989.3:p.Asn1135Tyr