Canonical Allele Identifier: CA366389289

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470076C>A (hg19) ; chr6:g.157148942C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148942C>A , CM000668.2:g.157148942C>A	GRCh38
NC_000006.11:g.157470076C>A , CM000668.1:g.157470076C>A	GRCh37
NC_000006.10:g.157511768C>A	NCBI36
NG_032093.1:g.376013C>A
NG_032093.2:g.376013C>A
NG_066624.1:g.377917C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3080C>A	ENSP00000055163.8:p.Ala1027Glu
ENST00000414678.8:c.2990C>A	ENSP00000412835.3:p.Ala997Glu
ENST00000637015.2:c.3080C>A	ENSP00000489729.2:p.Ala1027Glu
ENST00000319584.11:c.1094C>A	ENSP00000313006.7:p.Ala365Glu
ENST00000346085.10:c.3119C>A	ENSP00000344546.5:p.Ala1040Glu
ENST00000350026.10:c.2831C>A	ENSP00000055163.7:p.Ala944Glu
ENST00000414678.7:c.1238C>A	ENSP00000412835.2:p.Ala413Glu
ENST00000452544.2:n.981C>A
ENST00000635849.1:c.401C>A	ENSP00000490948.1:p.Ala134Glu
ENST00000635957.1:c.35C>A	ENSP00000490385.1:p.Ala12Glu
ENST00000636426.1:n.214C>A
ENST00000636930.2:c.3080C>A MANE Select	ENSP00000490491.2:p.Ala1027Glu
ENST00000637015.1:c.319C>A
ENST00000637568.1:c.123C>A
ENST00000637810.1:c.581C>A	ENSP00000489636.1:p.Ala194Glu
ENST00000637904.1:c.581C>A	ENSP00000490550.1:p.Ala194Glu
ENST00000647938.1:c.2870C>A	ENSP00000498155.1:p.Ala957Glu
ENST00000674190.1:n.1829C>A
ENST00000319584.10:c.1097C>A	ENSP00000313006.6:p.Ala366Glu
ENST00000346085.9:c.2870C>A	ENSP00000344546.4:p.Ala957Glu
ENST00000350026.9:c.2831C>A	ENSP00000055163.7:p.Ala944Glu
ENST00000400790.3:c.32C>A	ENSP00000383596.3:p.Ala11Glu
ENST00000414678.6:c.1238C>A	ENSP00000412835.2:p.Ala413Glu
ENST00000452544.1:n.927C>A
ENST00000478761.3:c.153C>A
NM_017519.2:c.2831C>A	NP_059989.2:p.Ala944Glu
NM_020732.3:c.2870C>A	NP_065783.3:p.Ala957Glu
XM_005267069.3:c.2831C>A	XP_005267126.2:p.Ala944Glu
XM_011535984.1:c.1781C>A	XP_011534286.1:p.Ala594Glu
XM_011535985.1:c.1601C>A	XP_011534287.1:p.Ala534Glu
XM_011535986.1:c.1361C>A	XP_011534288.1:p.Ala454Glu
XM_011535987.1:c.980C>A	XP_011534289.1:p.Ala327Glu
XM_011535988.1:c.-20+15735C>A	XP_011534290.1:n.-20+15735C>A
NM_001346813.1:c.2831C>A	NP_001333742.1:p.Ala944Glu
NM_001363725.1:c.581C>A	NP_001350654.1:p.Ala194Glu
XM_011535984.2:c.2912C>A	XP_011534286.2:p.Ala971Glu
XM_011535988.3:c.-20+15735C>A	XP_011534290.1:n.-20+15735C>A
XM_017011103.2:c.2912C>A	XP_016866592.1:p.Ala971Glu
XM_017011104.1:c.2912C>A	XP_016866593.1:p.Ala971Glu
XM_017011105.2:c.2912C>A	XP_016866594.1:p.Ala971Glu
XM_017011106.2:c.2912C>A	XP_016866595.1:p.Ala971Glu
XM_017011107.2:c.2732C>A	XP_016866596.1:p.Ala911Glu
XR_002956289.1:n.2995C>A
NM_001363725.2:c.581C>A	NP_001350654.1:p.Ala194Glu
NM_001371656.1:c.3119C>A	NP_001358585.1:p.Ala1040Glu
NM_001374820.1:c.3119C>A	NP_001361749.1:p.Ala1040Glu
NM_001374828.1:c.3080C>A MANE Select	NP_001361757.1:p.Ala1027Glu
NM_017519.3:c.3080C>A	NP_059989.3:p.Ala1027Glu