Canonical Allele Identifier: CA452784341

Gene: ARID1B

Linked Data

• dbSNP Id: rs1400239215
• gnomAD v3: 6-157200773-C-T
• gnomAD v4: 6-157200773-C-T
• MyVariant Identifiers: chr6:g.157521907C>T (hg19) ; chr6:g.157200773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200773C>T , CM000668.2:g.157200773C>T	GRCh38
NC_000006.11:g.157521907C>T , CM000668.1:g.157521907C>T	GRCh37
NC_000006.10:g.157563599C>T	NCBI36
NG_032093.1:g.427844C>T
NG_032093.2:g.427844C>T
NG_066624.1:g.429748C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4389C>T	ENSP00000055163.8:p.Asn1463=
ENST00000414678.8:c.4458C>T	ENSP00000412835.3:p.Asn1486=
ENST00000637015.2:c.4677C>T	ENSP00000489729.2:p.Asn1559=
ENST00000346085.10:c.4428C>T	ENSP00000344546.5:p.Asn1476=
ENST00000350026.10:c.4140C>T	ENSP00000055163.7:p.Asn1380=
ENST00000414678.7:c.2706C>T	ENSP00000412835.2:p.Asn902=
ENST00000635849.1:c.1869C>T	ENSP00000490948.1:p.Asn623=
ENST00000635957.1:c.1500C>T	ENSP00000490385.1:p.Asn500=
ENST00000636227.1:n.3011C>T
ENST00000636254.1:n.468C>T
ENST00000636930.2:c.4548C>T MANE Select	ENSP00000490491.2:p.Asn1516=
ENST00000636940.1:n.2545C>T
ENST00000637015.1:c.1916C>T
ENST00000637568.1:c.1830C>T
ENST00000637741.1:n.1214C>T
ENST00000637810.1:c.1890C>T	ENSP00000489636.1:p.Asn630=
ENST00000637904.1:c.2049C>T	ENSP00000490550.1:p.Asn683=
ENST00000647938.1:c.4179C>T	ENSP00000498155.1:p.Asn1393=
ENST00000346085.9:c.4179C>T	ENSP00000344546.4:p.Asn1393=
ENST00000350026.9:c.4140C>T	ENSP00000055163.7:p.Asn1380=
ENST00000414678.6:c.2706C>T	ENSP00000412835.2:p.Asn902=
NM_017519.2:c.4140C>T	NP_059989.2:p.Asn1380=
NM_020732.3:c.4179C>T	NP_065783.3:p.Asn1393=
XM_005267069.3:c.4299C>T	XP_005267126.2:p.Asn1433=
XM_011535984.1:c.3378C>T	XP_011534286.1:p.Asn1126=
XM_011535985.1:c.3198C>T	XP_011534287.1:p.Asn1066=
XM_011535986.1:c.2958C>T	XP_011534288.1:p.Asn986=
XM_011535987.1:c.2577C>T	XP_011534289.1:p.Asn859=
XM_011535988.1:c.1440C>T	XP_011534290.1:p.Asn480=
NM_001346813.1:c.4299C>T	NP_001333742.1:p.Asn1433=
NM_001363725.1:c.2049C>T	NP_001350654.1:p.Asn683=
XM_011535984.2:c.4509C>T	XP_011534286.2:p.Asn1503=
XM_011535988.3:c.1440C>T	XP_011534290.1:p.Asn480=
XM_017011103.2:c.4410C>T	XP_016866592.1:p.Asn1470=
XM_017011104.1:c.4380C>T	XP_016866593.1:p.Asn1460=
XM_017011105.2:c.4350C>T	XP_016866594.1:p.Asn1450=
XM_017011106.2:c.4221C>T	XP_016866595.1:p.Asn1407=
XM_017011107.2:c.4200C>T	XP_016866596.1:p.Asn1400=
XR_002956289.1:n.4495C>T
NM_001363725.2:c.2049C>T	NP_001350654.1:p.Asn683=
NM_001371656.1:c.4428C>T	NP_001358585.1:p.Asn1476=
NM_001374820.1:c.4428C>T	NP_001361749.1:p.Asn1476=
NM_001374828.1:c.4548C>T MANE Select	NP_001361757.1:p.Asn1516=
NM_017519.3:c.4389C>T	NP_059989.3:p.Asn1463=