Canonical Allele Identifier: CA366389291

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3080C>G	ENSP00000055163.8:p.Ala1027Gly
ENST00000414678.8:c.2990C>G	ENSP00000412835.3:p.Ala997Gly
ENST00000637015.2:c.3080C>G	ENSP00000489729.2:p.Ala1027Gly
ENST00000319584.11:c.1094C>G	ENSP00000313006.7:p.Ala365Gly
ENST00000346085.10:c.3119C>G	ENSP00000344546.5:p.Ala1040Gly
ENST00000350026.10:c.2831C>G	ENSP00000055163.7:p.Ala944Gly
ENST00000414678.7:c.1238C>G	ENSP00000412835.2:p.Ala413Gly
ENST00000452544.2:n.981C>G
ENST00000635849.1:c.401C>G	ENSP00000490948.1:p.Ala134Gly
ENST00000635957.1:c.35C>G	ENSP00000490385.1:p.Ala12Gly
ENST00000636426.1:n.214C>G
ENST00000636930.2:c.3080C>G MANE Select	ENSP00000490491.2:p.Ala1027Gly
ENST00000637015.1:c.319C>G
ENST00000637568.1:c.123C>G
ENST00000637810.1:c.581C>G	ENSP00000489636.1:p.Ala194Gly
ENST00000637904.1:c.581C>G	ENSP00000490550.1:p.Ala194Gly
ENST00000647938.1:c.2870C>G	ENSP00000498155.1:p.Ala957Gly
ENST00000674190.1:n.1829C>G
ENST00000319584.10:c.1097C>G	ENSP00000313006.6:p.Ala366Gly
ENST00000346085.9:c.2870C>G	ENSP00000344546.4:p.Ala957Gly
ENST00000350026.9:c.2831C>G	ENSP00000055163.7:p.Ala944Gly
ENST00000400790.3:c.32C>G	ENSP00000383596.3:p.Ala11Gly
ENST00000414678.6:c.1238C>G	ENSP00000412835.2:p.Ala413Gly
ENST00000452544.1:n.927C>G
ENST00000478761.3:c.153C>G
NM_017519.2:c.2831C>G	NP_059989.2:p.Ala944Gly
NM_020732.3:c.2870C>G	NP_065783.3:p.Ala957Gly
XM_005267069.3:c.2831C>G	XP_005267126.2:p.Ala944Gly
XM_011535984.1:c.1781C>G	XP_011534286.1:p.Ala594Gly
XM_011535985.1:c.1601C>G	XP_011534287.1:p.Ala534Gly
XM_011535986.1:c.1361C>G	XP_011534288.1:p.Ala454Gly
XM_011535987.1:c.980C>G	XP_011534289.1:p.Ala327Gly
XM_011535988.1:c.-20+15735C>G	XP_011534290.1:n.-20+15735C>G
NM_001346813.1:c.2831C>G	NP_001333742.1:p.Ala944Gly
NM_001363725.1:c.581C>G	NP_001350654.1:p.Ala194Gly
XM_011535984.2:c.2912C>G	XP_011534286.2:p.Ala971Gly
XM_011535988.3:c.-20+15735C>G	XP_011534290.1:n.-20+15735C>G
XM_017011103.2:c.2912C>G	XP_016866592.1:p.Ala971Gly
XM_017011104.1:c.2912C>G	XP_016866593.1:p.Ala971Gly
XM_017011105.2:c.2912C>G	XP_016866594.1:p.Ala971Gly
XM_017011106.2:c.2912C>G	XP_016866595.1:p.Ala971Gly
XM_017011107.2:c.2732C>G	XP_016866596.1:p.Ala911Gly
XR_002956289.1:n.2995C>G
NM_001363725.2:c.581C>G	NP_001350654.1:p.Ala194Gly
NM_001371656.1:c.3119C>G	NP_001358585.1:p.Ala1040Gly
NM_001374820.1:c.3119C>G	NP_001361749.1:p.Ala1040Gly
NM_001374828.1:c.3080C>G MANE Select	NP_001361757.1:p.Ala1027Gly
NM_017519.3:c.3080C>G	NP_059989.3:p.Ala1027Gly