Canonical Allele Identifier: CA366389208

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470037A>C (hg19) ; chr6:g.157148903A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148903A>C , CM000668.2:g.157148903A>C	GRCh38
NC_000006.11:g.157470037A>C , CM000668.1:g.157470037A>C	GRCh37
NC_000006.10:g.157511729A>C	NCBI36
NG_032093.1:g.375974A>C
NG_032093.2:g.375974A>C
NG_066624.1:g.377878A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3041A>C	ENSP00000055163.8:p.Glu1014Ala
ENST00000414678.8:c.2951A>C	ENSP00000412835.3:p.Glu984Ala
ENST00000637015.2:c.3041A>C	ENSP00000489729.2:p.Glu1014Ala
ENST00000319584.11:c.1055A>C	ENSP00000313006.7:p.Glu352Ala
ENST00000346085.10:c.3080A>C	ENSP00000344546.5:p.Glu1027Ala
ENST00000350026.10:c.2792A>C	ENSP00000055163.7:p.Glu931Ala
ENST00000414678.7:c.1199A>C	ENSP00000412835.2:p.Glu400Ala
ENST00000452544.2:n.942A>C
ENST00000635849.1:c.362A>C	ENSP00000490948.1:p.Glu121Ala
ENST00000636426.1:n.175A>C
ENST00000636930.2:c.3041A>C MANE Select	ENSP00000490491.2:p.Glu1014Ala
ENST00000637015.1:c.280A>C
ENST00000637568.1:c.84A>C
ENST00000637810.1:c.542A>C	ENSP00000489636.1:p.Glu181Ala
ENST00000637904.1:c.542A>C	ENSP00000490550.1:p.Glu181Ala
ENST00000647938.1:c.2831A>C	ENSP00000498155.1:p.Glu944Ala
ENST00000674190.1:n.1790A>C
ENST00000319584.10:c.1058A>C	ENSP00000313006.6:p.Glu353Ala
ENST00000346085.9:c.2831A>C	ENSP00000344546.4:p.Glu944Ala
ENST00000350026.9:c.2792A>C	ENSP00000055163.7:p.Glu931Ala
ENST00000414678.6:c.1199A>C	ENSP00000412835.2:p.Glu400Ala
ENST00000452544.1:n.888A>C
ENST00000478761.3:c.114A>C
NM_017519.2:c.2792A>C	NP_059989.2:p.Glu931Ala
NM_020732.3:c.2831A>C	NP_065783.3:p.Glu944Ala
XM_005267069.3:c.2792A>C	XP_005267126.2:p.Glu931Ala
XM_011535984.1:c.1742A>C	XP_011534286.1:p.Glu581Ala
XM_011535985.1:c.1562A>C	XP_011534287.1:p.Glu521Ala
XM_011535986.1:c.1322A>C	XP_011534288.1:p.Glu441Ala
XM_011535987.1:c.941A>C	XP_011534289.1:p.Glu314Ala
XM_011535988.1:c.-20+15696A>C	XP_011534290.1:n.-20+15696A>C
NM_001346813.1:c.2792A>C	NP_001333742.1:p.Glu931Ala
NM_001363725.1:c.542A>C	NP_001350654.1:p.Glu181Ala
XM_011535984.2:c.2873A>C	XP_011534286.2:p.Glu958Ala
XM_011535988.3:c.-20+15696A>C	XP_011534290.1:n.-20+15696A>C
XM_017011103.2:c.2873A>C	XP_016866592.1:p.Glu958Ala
XM_017011104.1:c.2873A>C	XP_016866593.1:p.Glu958Ala
XM_017011105.2:c.2873A>C	XP_016866594.1:p.Glu958Ala
XM_017011106.2:c.2873A>C	XP_016866595.1:p.Glu958Ala
XM_017011107.2:c.2693A>C	XP_016866596.1:p.Glu898Ala
XR_002956289.1:n.2956A>C
NM_001363725.2:c.542A>C	NP_001350654.1:p.Glu181Ala
NM_001371656.1:c.3080A>C	NP_001358585.1:p.Glu1027Ala
NM_001374820.1:c.3080A>C	NP_001361749.1:p.Glu1027Ala
NM_001374828.1:c.3041A>C MANE Select	NP_001361757.1:p.Glu1014Ala
NM_017519.3:c.3041A>C	NP_059989.3:p.Glu1014Ala