Canonical Allele Identifier: CA366234100

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189693-A-G
• MyVariant Identifiers: chr6:g.157510827A>G (hg19) ; chr6:g.157189693A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189693A>G , CM000668.2:g.157189693A>G	GRCh38
NC_000006.11:g.157510827A>G , CM000668.1:g.157510827A>G	GRCh37
NC_000006.10:g.157552519A>G	NCBI36
NG_032093.1:g.416764A>G
NG_032093.2:g.416764A>G
NG_066624.1:g.418668A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3812A>G	ENSP00000055163.8:p.Asn1271Ser
ENST00000414678.8:c.3881A>G	ENSP00000412835.3:p.Asn1294Ser
ENST00000637015.2:c.4100A>G	ENSP00000489729.2:p.Asn1367Ser
ENST00000346085.10:c.3851A>G	ENSP00000344546.5:p.Asn1284Ser
ENST00000350026.10:c.3563A>G	ENSP00000055163.7:p.Asn1188Ser
ENST00000414678.7:c.2129A>G	ENSP00000412835.2:p.Asn710Ser
ENST00000635849.1:c.1292A>G	ENSP00000490948.1:p.Asn431Ser
ENST00000635957.1:c.926A>G	ENSP00000490385.1:p.Asn309Ser
ENST00000636930.2:c.3971A>G MANE Select	ENSP00000490491.2:p.Asn1324Ser
ENST00000636940.1:n.1968A>G
ENST00000637015.1:c.1339A>G
ENST00000637568.1:c.1253A>G
ENST00000637741.1:n.637A>G
ENST00000637810.1:c.1313A>G	ENSP00000489636.1:p.Asn438Ser
ENST00000637904.1:c.1472A>G	ENSP00000490550.1:p.Asn491Ser
ENST00000647938.1:c.3602A>G	ENSP00000498155.1:p.Asn1201Ser
ENST00000346085.9:c.3602A>G	ENSP00000344546.4:p.Asn1201Ser
ENST00000350026.9:c.3563A>G	ENSP00000055163.7:p.Asn1188Ser
ENST00000414678.6:c.2129A>G	ENSP00000412835.2:p.Asn710Ser
NM_017519.2:c.3563A>G	NP_059989.2:p.Asn1188Ser
NM_020732.3:c.3602A>G	NP_065783.3:p.Asn1201Ser
XM_005267069.3:c.3722A>G	XP_005267126.2:p.Asn1241Ser
XM_011535984.1:c.2801A>G	XP_011534286.1:p.Asn934Ser
XM_011535985.1:c.2621A>G	XP_011534287.1:p.Asn874Ser
XM_011535986.1:c.2381A>G	XP_011534288.1:p.Asn794Ser
XM_011535987.1:c.2000A>G	XP_011534289.1:p.Asn667Ser
XM_011535988.1:c.863A>G	XP_011534290.1:p.Asn288Ser
NM_001346813.1:c.3722A>G	NP_001333742.1:p.Asn1241Ser
NM_001363725.1:c.1472A>G	NP_001350654.1:p.Asn491Ser
XM_011535984.2:c.3932A>G	XP_011534286.2:p.Asn1311Ser
XM_011535988.3:c.863A>G	XP_011534290.1:p.Asn288Ser
XM_017011103.2:c.3833A>G	XP_016866592.1:p.Asn1278Ser
XM_017011104.1:c.3803A>G	XP_016866593.1:p.Asn1268Ser
XM_017011105.2:c.3773A>G	XP_016866594.1:p.Asn1258Ser
XM_017011106.2:c.3644A>G	XP_016866595.1:p.Asn1215Ser
XM_017011107.2:c.3623A>G	XP_016866596.1:p.Asn1208Ser
XR_002956289.1:n.4015A>G
NM_001363725.2:c.1472A>G	NP_001350654.1:p.Asn491Ser
NM_001371656.1:c.3851A>G	NP_001358585.1:p.Asn1284Ser
NM_001374820.1:c.3851A>G	NP_001361749.1:p.Asn1284Ser
NM_001374828.1:c.3971A>G MANE Select	NP_001361757.1:p.Asn1324Ser
NM_017519.3:c.3812A>G	NP_059989.3:p.Asn1271Ser