Canonical Allele Identifier: CA452781862

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511238C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190104C>T , CM000668.2:g.157190104C>T	GRCh38
NC_000006.11:g.157511238C>T , CM000668.1:g.157511238C>T	GRCh37
NC_000006.10:g.157552930C>T	NCBI36
NG_032093.1:g.417175C>T
NG_032093.2:g.417175C>T
NG_066624.1:g.419079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3966C>T	ENSP00000055163.8:p.Asn1322=
ENST00000414678.8:c.4035C>T	ENSP00000412835.3:p.Asn1345=
ENST00000637015.2:c.4254C>T	ENSP00000489729.2:p.Asn1418=
ENST00000346085.10:c.4005C>T	ENSP00000344546.5:p.Asn1335=
ENST00000350026.10:c.3717C>T	ENSP00000055163.7:p.Asn1239=
ENST00000414678.7:c.2283C>T	ENSP00000412835.2:p.Asn761=
ENST00000635849.1:c.1446C>T	ENSP00000490948.1:p.Asn482=
ENST00000635957.1:c.1077C>T	ENSP00000490385.1:p.Asn359=
ENST00000636930.2:c.4125C>T MANE Select	ENSP00000490491.2:p.Asn1375=
ENST00000636940.1:n.2122C>T
ENST00000637015.1:c.1493C>T
ENST00000637568.1:c.1407C>T
ENST00000637741.1:n.791C>T
ENST00000637810.1:c.1467C>T	ENSP00000489636.1:p.Asn489=
ENST00000637904.1:c.1626C>T	ENSP00000490550.1:p.Asn542=
ENST00000647938.1:c.3756C>T	ENSP00000498155.1:p.Asn1252=
ENST00000346085.9:c.3756C>T	ENSP00000344546.4:p.Asn1252=
ENST00000350026.9:c.3717C>T	ENSP00000055163.7:p.Asn1239=
ENST00000414678.6:c.2283C>T	ENSP00000412835.2:p.Asn761=
NM_017519.2:c.3717C>T	NP_059989.2:p.Asn1239=
NM_020732.3:c.3756C>T	NP_065783.3:p.Asn1252=
XM_005267069.3:c.3876C>T	XP_005267126.2:p.Asn1292=
XM_011535984.1:c.2955C>T	XP_011534286.1:p.Asn985=
XM_011535985.1:c.2775C>T	XP_011534287.1:p.Asn925=
XM_011535986.1:c.2535C>T	XP_011534288.1:p.Asn845=
XM_011535987.1:c.2154C>T	XP_011534289.1:p.Asn718=
XM_011535988.1:c.1017C>T	XP_011534290.1:p.Asn339=
NM_001346813.1:c.3876C>T	NP_001333742.1:p.Asn1292=
NM_001363725.1:c.1626C>T	NP_001350654.1:p.Asn542=
XM_011535984.2:c.4086C>T	XP_011534286.2:p.Asn1362=
XM_011535988.3:c.1017C>T	XP_011534290.1:p.Asn339=
XM_017011103.2:c.3987C>T	XP_016866592.1:p.Asn1329=
XM_017011104.1:c.3957C>T	XP_016866593.1:p.Asn1319=
XM_017011105.2:c.3927C>T	XP_016866594.1:p.Asn1309=
XM_017011106.2:c.3798C>T	XP_016866595.1:p.Asn1266=
XM_017011107.2:c.3777C>T	XP_016866596.1:p.Asn1259=
XR_002956289.1:n.4169C>T
NM_001363725.2:c.1626C>T	NP_001350654.1:p.Asn542=
NM_001371656.1:c.4005C>T	NP_001358585.1:p.Asn1335=
NM_001374820.1:c.4005C>T	NP_001361749.1:p.Asn1335=
NM_001374828.1:c.4125C>T MANE Select	NP_001361757.1:p.Asn1375=
NM_017519.3:c.3966C>T	NP_059989.3:p.Asn1322=