Canonical Allele Identifier: CA366227584

Gene: ARID1B

Linked Data

• dbSNP Id: rs761227259
• gnomAD v4: 6-157181053-G-T
• MyVariant Identifiers: chr6:g.157502187G>T (hg19) ; chr6:g.157181053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181053G>T , CM000668.2:g.157181053G>T	GRCh38
NC_000006.11:g.157502187G>T , CM000668.1:g.157502187G>T	GRCh37
NC_000006.10:g.157543879G>T	NCBI36
NG_032093.1:g.408124G>T
NG_032093.2:g.408124G>T
NG_066624.1:g.410028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3430G>T	ENSP00000055163.8:p.Asp1144Tyr
ENST00000414678.8:c.3499G>T	ENSP00000412835.3:p.Asp1167Tyr
ENST00000637015.2:c.3718G>T	ENSP00000489729.2:p.Asp1240Tyr
ENST00000319584.11:c.1603G>T	ENSP00000313006.7:p.Asp535Tyr
ENST00000346085.10:c.3469G>T	ENSP00000344546.5:p.Asp1157Tyr
ENST00000350026.10:c.3181G>T	ENSP00000055163.7:p.Asp1061Tyr
ENST00000414678.7:c.1747G>T	ENSP00000412835.2:p.Asp583Tyr
ENST00000635849.1:c.910G>T	ENSP00000490948.1:p.Asp304Tyr
ENST00000635957.1:c.544G>T	ENSP00000490385.1:p.Asp182Tyr
ENST00000636930.2:c.3589G>T MANE Select	ENSP00000490491.2:p.Asp1197Tyr
ENST00000636940.1:n.1586G>T
ENST00000637015.1:c.957G>T
ENST00000637568.1:c.871G>T
ENST00000637741.1:n.255G>T
ENST00000637810.1:c.931G>T	ENSP00000489636.1:p.Asp311Tyr
ENST00000637904.1:c.1090G>T	ENSP00000490550.1:p.Asp364Tyr
ENST00000647938.1:c.3220G>T	ENSP00000498155.1:p.Asp1074Tyr
ENST00000319584.10:c.1606G>T	ENSP00000313006.6:p.Asp536Tyr
ENST00000346085.9:c.3220G>T	ENSP00000344546.4:p.Asp1074Tyr
ENST00000350026.9:c.3181G>T	ENSP00000055163.7:p.Asp1061Tyr
ENST00000400790.3:c.382G>T	ENSP00000383596.3:p.Asp128Tyr
ENST00000414678.6:c.1747G>T	ENSP00000412835.2:p.Asp583Tyr
ENST00000478761.3:c.791G>T
NM_017519.2:c.3181G>T	NP_059989.2:p.Asp1061Tyr
NM_020732.3:c.3220G>T	NP_065783.3:p.Asp1074Tyr
XM_005267069.3:c.3340G>T	XP_005267126.2:p.Asp1114Tyr
XM_011535984.1:c.2419G>T	XP_011534286.1:p.Asp807Tyr
XM_011535985.1:c.2239G>T	XP_011534287.1:p.Asp747Tyr
XM_011535986.1:c.1999G>T	XP_011534288.1:p.Asp667Tyr
XM_011535987.1:c.1618G>T	XP_011534289.1:p.Asp540Tyr
XM_011535988.1:c.481G>T	XP_011534290.1:p.Asp161Tyr
NM_001346813.1:c.3340G>T	NP_001333742.1:p.Asp1114Tyr
NM_001363725.1:c.1090G>T	NP_001350654.1:p.Asp364Tyr
XM_011535984.2:c.3550G>T	XP_011534286.2:p.Asp1184Tyr
XM_011535988.3:c.481G>T	XP_011534290.1:p.Asp161Tyr
XM_017011103.2:c.3451G>T	XP_016866592.1:p.Asp1151Tyr
XM_017011104.1:c.3421G>T	XP_016866593.1:p.Asp1141Tyr
XM_017011105.2:c.3391G>T	XP_016866594.1:p.Asp1131Tyr
XM_017011106.2:c.3262G>T	XP_016866595.1:p.Asp1088Tyr
XM_017011107.2:c.3241G>T	XP_016866596.1:p.Asp1081Tyr
XR_002956289.1:n.3633G>T
NM_001363725.2:c.1090G>T	NP_001350654.1:p.Asp364Tyr
NM_001371656.1:c.3469G>T	NP_001358585.1:p.Asp1157Tyr
NM_001374820.1:c.3469G>T	NP_001361749.1:p.Asp1157Tyr
NM_001374828.1:c.3589G>T MANE Select	NP_001361757.1:p.Asp1197Tyr
NM_017519.3:c.3430G>T	NP_059989.3:p.Asp1144Tyr