Canonical Allele Identifier: CA452990098

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470038G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148904G>A , CM000668.2:g.157148904G>A	GRCh38
NC_000006.11:g.157470038G>A , CM000668.1:g.157470038G>A	GRCh37
NC_000006.10:g.157511730G>A	NCBI36
NG_032093.1:g.375975G>A
NG_032093.2:g.375975G>A
NG_066624.1:g.377879G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3042G>A	ENSP00000055163.8:p.Glu1014=
ENST00000414678.8:c.2952G>A	ENSP00000412835.3:p.Glu984=
ENST00000637015.2:c.3042G>A	ENSP00000489729.2:p.Glu1014=
ENST00000319584.11:c.1056G>A	ENSP00000313006.7:p.Glu352=
ENST00000346085.10:c.3081G>A	ENSP00000344546.5:p.Glu1027=
ENST00000350026.10:c.2793G>A	ENSP00000055163.7:p.Glu931=
ENST00000414678.7:c.1200G>A	ENSP00000412835.2:p.Glu400=
ENST00000452544.2:n.943G>A
ENST00000635849.1:c.363G>A	ENSP00000490948.1:p.Glu121=
ENST00000636426.1:n.176G>A
ENST00000636930.2:c.3042G>A MANE Select	ENSP00000490491.2:p.Glu1014=
ENST00000637015.1:c.281G>A
ENST00000637568.1:c.85G>A
ENST00000637810.1:c.543G>A	ENSP00000489636.1:p.Glu181=
ENST00000637904.1:c.543G>A	ENSP00000490550.1:p.Glu181=
ENST00000647938.1:c.2832G>A	ENSP00000498155.1:p.Glu944=
ENST00000674190.1:n.1791G>A
ENST00000319584.10:c.1059G>A	ENSP00000313006.6:p.Glu353=
ENST00000346085.9:c.2832G>A	ENSP00000344546.4:p.Glu944=
ENST00000350026.9:c.2793G>A	ENSP00000055163.7:p.Glu931=
ENST00000414678.6:c.1200G>A	ENSP00000412835.2:p.Glu400=
ENST00000452544.1:n.889G>A
ENST00000478761.3:c.115G>A
NM_017519.2:c.2793G>A	NP_059989.2:p.Glu931=
NM_020732.3:c.2832G>A	NP_065783.3:p.Glu944=
XM_005267069.3:c.2793G>A	XP_005267126.2:p.Glu931=
XM_011535984.1:c.1743G>A	XP_011534286.1:p.Glu581=
XM_011535985.1:c.1563G>A	XP_011534287.1:p.Glu521=
XM_011535986.1:c.1323G>A	XP_011534288.1:p.Glu441=
XM_011535987.1:c.942G>A	XP_011534289.1:p.Glu314=
XM_011535988.1:c.-20+15697G>A	XP_011534290.1:n.-20+15697G>A
NM_001346813.1:c.2793G>A	NP_001333742.1:p.Glu931=
NM_001363725.1:c.543G>A	NP_001350654.1:p.Glu181=
XM_011535984.2:c.2874G>A	XP_011534286.2:p.Glu958=
XM_011535988.3:c.-20+15697G>A	XP_011534290.1:n.-20+15697G>A
XM_017011103.2:c.2874G>A	XP_016866592.1:p.Glu958=
XM_017011104.1:c.2874G>A	XP_016866593.1:p.Glu958=
XM_017011105.2:c.2874G>A	XP_016866594.1:p.Glu958=
XM_017011106.2:c.2874G>A	XP_016866595.1:p.Glu958=
XM_017011107.2:c.2694G>A	XP_016866596.1:p.Glu898=
XR_002956289.1:n.2957G>A
NM_001363725.2:c.543G>A	NP_001350654.1:p.Glu181=
NM_001371656.1:c.3081G>A	NP_001358585.1:p.Glu1027=
NM_001374820.1:c.3081G>A	NP_001361749.1:p.Glu1027=
NM_001374828.1:c.3042G>A MANE Select	NP_001361757.1:p.Glu1014=
NM_017519.3:c.3042G>A	NP_059989.3:p.Glu1014=