Canonical Allele Identifier: CA452780768

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317167
• MyVariant Identifiers: chr6:g.157502198C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181064C>G , CM000668.2:g.157181064C>G	GRCh38
NC_000006.11:g.157502198C>G , CM000668.1:g.157502198C>G	GRCh37
NC_000006.10:g.157543890C>G	NCBI36
NG_032093.1:g.408135C>G
NG_032093.2:g.408135C>G
NG_066624.1:g.410039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3441C>G	ENSP00000055163.8:p.Leu1147=
ENST00000414678.8:c.3510C>G	ENSP00000412835.3:p.Leu1170=
ENST00000637015.2:c.3729C>G	ENSP00000489729.2:p.Leu1243=
ENST00000319584.11:c.1614C>G	ENSP00000313006.7:p.Leu538=
ENST00000346085.10:c.3480C>G	ENSP00000344546.5:p.Leu1160=
ENST00000350026.10:c.3192C>G	ENSP00000055163.7:p.Leu1064=
ENST00000414678.7:c.1758C>G	ENSP00000412835.2:p.Leu586=
ENST00000635849.1:c.921C>G	ENSP00000490948.1:p.Leu307=
ENST00000635957.1:c.555C>G	ENSP00000490385.1:p.Leu185=
ENST00000636930.2:c.3600C>G MANE Select	ENSP00000490491.2:p.Leu1200=
ENST00000636940.1:n.1597C>G
ENST00000637015.1:c.968C>G
ENST00000637568.1:c.882C>G
ENST00000637741.1:n.266C>G
ENST00000637810.1:c.942C>G	ENSP00000489636.1:p.Leu314=
ENST00000637904.1:c.1101C>G	ENSP00000490550.1:p.Leu367=
ENST00000647938.1:c.3231C>G	ENSP00000498155.1:p.Leu1077=
ENST00000319584.10:c.1617C>G	ENSP00000313006.6:p.Leu539=
ENST00000346085.9:c.3231C>G	ENSP00000344546.4:p.Leu1077=
ENST00000350026.9:c.3192C>G	ENSP00000055163.7:p.Leu1064=
ENST00000400790.3:c.393C>G	ENSP00000383596.3:p.Leu131=
ENST00000414678.6:c.1758C>G	ENSP00000412835.2:p.Leu586=
ENST00000478761.3:c.802C>G
NM_017519.2:c.3192C>G	NP_059989.2:p.Leu1064=
NM_020732.3:c.3231C>G	NP_065783.3:p.Leu1077=
XM_005267069.3:c.3351C>G	XP_005267126.2:p.Leu1117=
XM_011535984.1:c.2430C>G	XP_011534286.1:p.Leu810=
XM_011535985.1:c.2250C>G	XP_011534287.1:p.Leu750=
XM_011535986.1:c.2010C>G	XP_011534288.1:p.Leu670=
XM_011535987.1:c.1629C>G	XP_011534289.1:p.Leu543=
XM_011535988.1:c.492C>G	XP_011534290.1:p.Leu164=
NM_001346813.1:c.3351C>G	NP_001333742.1:p.Leu1117=
NM_001363725.1:c.1101C>G	NP_001350654.1:p.Leu367=
XM_011535984.2:c.3561C>G	XP_011534286.2:p.Leu1187=
XM_011535988.3:c.492C>G	XP_011534290.1:p.Leu164=
XM_017011103.2:c.3462C>G	XP_016866592.1:p.Leu1154=
XM_017011104.1:c.3432C>G	XP_016866593.1:p.Leu1144=
XM_017011105.2:c.3402C>G	XP_016866594.1:p.Leu1134=
XM_017011106.2:c.3273C>G	XP_016866595.1:p.Leu1091=
XM_017011107.2:c.3252C>G	XP_016866596.1:p.Leu1084=
XR_002956289.1:n.3644C>G
NM_001363725.2:c.1101C>G	NP_001350654.1:p.Leu367=
NM_001371656.1:c.3480C>G	NP_001358585.1:p.Leu1160=
NM_001374820.1:c.3480C>G	NP_001361749.1:p.Leu1160=
NM_001374828.1:c.3600C>G MANE Select	NP_001361757.1:p.Leu1200=
NM_017519.3:c.3441C>G	NP_059989.3:p.Leu1147=