Canonical Allele Identifier: CA452780798

Gene: ARID1B

Linked Data

• dbSNP Id: rs746210543
• gnomAD v4: 6-157181109-C-G
• MyVariant Identifiers: chr6:g.157502243C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181109C>G , CM000668.2:g.157181109C>G	GRCh38
NC_000006.11:g.157502243C>G , CM000668.1:g.157502243C>G	GRCh37
NC_000006.10:g.157543935C>G	NCBI36
NG_032093.1:g.408180C>G
NG_032093.2:g.408180C>G
NG_066624.1:g.410084C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3486C>G	ENSP00000055163.8:p.Ala1162=
ENST00000414678.8:c.3555C>G	ENSP00000412835.3:p.Ala1185=
ENST00000637015.2:c.3774C>G	ENSP00000489729.2:p.Ala1258=
ENST00000319584.11:c.1659C>G	ENSP00000313006.7:p.Ala553=
ENST00000346085.10:c.3525C>G	ENSP00000344546.5:p.Ala1175=
ENST00000350026.10:c.3237C>G	ENSP00000055163.7:p.Ala1079=
ENST00000414678.7:c.1803C>G	ENSP00000412835.2:p.Ala601=
ENST00000635849.1:c.966C>G	ENSP00000490948.1:p.Ala322=
ENST00000635957.1:c.600C>G	ENSP00000490385.1:p.Ala200=
ENST00000636930.2:c.3645C>G MANE Select	ENSP00000490491.2:p.Ala1215=
ENST00000636940.1:n.1642C>G
ENST00000637015.1:c.1013C>G
ENST00000637568.1:c.927C>G
ENST00000637741.1:n.311C>G
ENST00000637810.1:c.987C>G	ENSP00000489636.1:p.Ala329=
ENST00000637904.1:c.1146C>G	ENSP00000490550.1:p.Ala382=
ENST00000647938.1:c.3276C>G	ENSP00000498155.1:p.Ala1092=
ENST00000319584.10:c.1662C>G	ENSP00000313006.6:p.Ala554=
ENST00000346085.9:c.3276C>G	ENSP00000344546.4:p.Ala1092=
ENST00000350026.9:c.3237C>G	ENSP00000055163.7:p.Ala1079=
ENST00000400790.3:c.438C>G	ENSP00000383596.3:p.Ala146=
ENST00000414678.6:c.1803C>G	ENSP00000412835.2:p.Ala601=
ENST00000478761.3:c.847C>G
NM_017519.2:c.3237C>G	NP_059989.2:p.Ala1079=
NM_020732.3:c.3276C>G	NP_065783.3:p.Ala1092=
XM_005267069.3:c.3396C>G	XP_005267126.2:p.Ala1132=
XM_011535984.1:c.2475C>G	XP_011534286.1:p.Ala825=
XM_011535985.1:c.2295C>G	XP_011534287.1:p.Ala765=
XM_011535986.1:c.2055C>G	XP_011534288.1:p.Ala685=
XM_011535987.1:c.1674C>G	XP_011534289.1:p.Ala558=
XM_011535988.1:c.537C>G	XP_011534290.1:p.Ala179=
NM_001346813.1:c.3396C>G	NP_001333742.1:p.Ala1132=
NM_001363725.1:c.1146C>G	NP_001350654.1:p.Ala382=
XM_011535984.2:c.3606C>G	XP_011534286.2:p.Ala1202=
XM_011535988.3:c.537C>G	XP_011534290.1:p.Ala179=
XM_017011103.2:c.3507C>G	XP_016866592.1:p.Ala1169=
XM_017011104.1:c.3477C>G	XP_016866593.1:p.Ala1159=
XM_017011105.2:c.3447C>G	XP_016866594.1:p.Ala1149=
XM_017011106.2:c.3318C>G	XP_016866595.1:p.Ala1106=
XM_017011107.2:c.3297C>G	XP_016866596.1:p.Ala1099=
XR_002956289.1:n.3689C>G
NM_001363725.2:c.1146C>G	NP_001350654.1:p.Ala382=
NM_001371656.1:c.3525C>G	NP_001358585.1:p.Ala1175=
NM_001374820.1:c.3525C>G	NP_001361749.1:p.Ala1175=
NM_001374828.1:c.3645C>G MANE Select	NP_001361757.1:p.Ala1215=
NM_017519.3:c.3486C>G	NP_059989.3:p.Ala1162=