Canonical Allele Identifier: CA452978256

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522405C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201271C>T , CM000668.2:g.157201271C>T	GRCh38
NC_000006.11:g.157522405C>T , CM000668.1:g.157522405C>T	GRCh37
NC_000006.10:g.157564097C>T	NCBI36
NG_032093.1:g.428342C>T
NG_032093.2:g.428342C>T
NG_066624.1:g.430246C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4887C>T	ENSP00000055163.8:p.Phe1629=
ENST00000414678.8:c.4956C>T	ENSP00000412835.3:p.Phe1652=
ENST00000637015.2:c.5175C>T	ENSP00000489729.2:p.Phe1725=
ENST00000346085.10:c.4926C>T	ENSP00000344546.5:p.Phe1642=
ENST00000350026.10:c.4638C>T	ENSP00000055163.7:p.Phe1546=
ENST00000414678.7:c.3204C>T	ENSP00000412835.2:p.Phe1068=
ENST00000635849.1:c.2367C>T	ENSP00000490948.1:p.Phe789=
ENST00000635957.1:c.1998C>T	ENSP00000490385.1:p.Phe666=
ENST00000636227.1:n.3509C>T
ENST00000636254.1:n.966C>T
ENST00000636930.2:c.5046C>T MANE Select	ENSP00000490491.2:p.Phe1682=
ENST00000636940.1:n.3043C>T
ENST00000637015.1:c.2414C>T
ENST00000637568.1:c.2328C>T
ENST00000637741.1:n.1712C>T
ENST00000637810.1:c.2388C>T	ENSP00000489636.1:p.Phe796=
ENST00000637904.1:c.2547C>T	ENSP00000490550.1:p.Phe849=
ENST00000647938.1:c.4677C>T	ENSP00000498155.1:p.Phe1559=
ENST00000346085.9:c.4677C>T	ENSP00000344546.4:p.Phe1559=
ENST00000350026.9:c.4638C>T	ENSP00000055163.7:p.Phe1546=
ENST00000414678.6:c.3204C>T	ENSP00000412835.2:p.Phe1068=
NM_017519.2:c.4638C>T	NP_059989.2:p.Phe1546=
NM_020732.3:c.4677C>T	NP_065783.3:p.Phe1559=
XM_005267069.3:c.4797C>T	XP_005267126.2:p.Phe1599=
XM_011535984.1:c.3876C>T	XP_011534286.1:p.Phe1292=
XM_011535985.1:c.3696C>T	XP_011534287.1:p.Phe1232=
XM_011535986.1:c.3456C>T	XP_011534288.1:p.Phe1152=
XM_011535987.1:c.3075C>T	XP_011534289.1:p.Phe1025=
XM_011535988.1:c.1938C>T	XP_011534290.1:p.Phe646=
NM_001346813.1:c.4797C>T	NP_001333742.1:p.Phe1599=
NM_001363725.1:c.2547C>T	NP_001350654.1:p.Phe849=
XM_011535984.2:c.5007C>T	XP_011534286.2:p.Phe1669=
XM_011535988.3:c.1938C>T	XP_011534290.1:p.Phe646=
XM_017011103.2:c.4908C>T	XP_016866592.1:p.Phe1636=
XM_017011104.1:c.4878C>T	XP_016866593.1:p.Phe1626=
XM_017011105.2:c.4848C>T	XP_016866594.1:p.Phe1616=
XM_017011106.2:c.4719C>T	XP_016866595.1:p.Phe1573=
XM_017011107.2:c.4698C>T	XP_016866596.1:p.Phe1566=
XR_002956289.1:n.4993C>T
NM_001363725.2:c.2547C>T	NP_001350654.1:p.Phe849=
NM_001371656.1:c.4926C>T	NP_001358585.1:p.Phe1642=
NM_001374820.1:c.4926C>T	NP_001361749.1:p.Phe1642=
NM_001374828.1:c.5046C>T MANE Select	NP_001361757.1:p.Phe1682=
NM_017519.3:c.4887C>T	NP_059989.3:p.Phe1629=