Canonical Allele Identifier: CA366241572

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522159C>G (hg19) ; chr6:g.157201025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201025C>G , CM000668.2:g.157201025C>G	GRCh38
NC_000006.11:g.157522159C>G , CM000668.1:g.157522159C>G	GRCh37
NC_000006.10:g.157563851C>G	NCBI36
NG_032093.1:g.428096C>G
NG_032093.2:g.428096C>G
NG_066624.1:g.430000C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4641C>G	ENSP00000055163.8:p.Asn1547Lys
ENST00000414678.8:c.4710C>G	ENSP00000412835.3:p.Asn1570Lys
ENST00000637015.2:c.4929C>G	ENSP00000489729.2:p.Asn1643Lys
ENST00000346085.10:c.4680C>G	ENSP00000344546.5:p.Asn1560Lys
ENST00000350026.10:c.4392C>G	ENSP00000055163.7:p.Asn1464Lys
ENST00000414678.7:c.2958C>G	ENSP00000412835.2:p.Asn986Lys
ENST00000635849.1:c.2121C>G	ENSP00000490948.1:p.Asn707Lys
ENST00000635957.1:c.1752C>G	ENSP00000490385.1:p.Asn584Lys
ENST00000636227.1:n.3263C>G
ENST00000636254.1:n.720C>G
ENST00000636930.2:c.4800C>G MANE Select	ENSP00000490491.2:p.Asn1600Lys
ENST00000636940.1:n.2797C>G
ENST00000637015.1:c.2168C>G
ENST00000637568.1:c.2082C>G
ENST00000637741.1:n.1466C>G
ENST00000637810.1:c.2142C>G	ENSP00000489636.1:p.Asn714Lys
ENST00000637904.1:c.2301C>G	ENSP00000490550.1:p.Asn767Lys
ENST00000647938.1:c.4431C>G	ENSP00000498155.1:p.Asn1477Lys
ENST00000346085.9:c.4431C>G	ENSP00000344546.4:p.Asn1477Lys
ENST00000350026.9:c.4392C>G	ENSP00000055163.7:p.Asn1464Lys
ENST00000414678.6:c.2958C>G	ENSP00000412835.2:p.Asn986Lys
NM_017519.2:c.4392C>G	NP_059989.2:p.Asn1464Lys
NM_020732.3:c.4431C>G	NP_065783.3:p.Asn1477Lys
XM_005267069.3:c.4551C>G	XP_005267126.2:p.Asn1517Lys
XM_011535984.1:c.3630C>G	XP_011534286.1:p.Asn1210Lys
XM_011535985.1:c.3450C>G	XP_011534287.1:p.Asn1150Lys
XM_011535986.1:c.3210C>G	XP_011534288.1:p.Asn1070Lys
XM_011535987.1:c.2829C>G	XP_011534289.1:p.Asn943Lys
XM_011535988.1:c.1692C>G	XP_011534290.1:p.Asn564Lys
NM_001346813.1:c.4551C>G	NP_001333742.1:p.Asn1517Lys
NM_001363725.1:c.2301C>G	NP_001350654.1:p.Asn767Lys
XM_011535984.2:c.4761C>G	XP_011534286.2:p.Asn1587Lys
XM_011535988.3:c.1692C>G	XP_011534290.1:p.Asn564Lys
XM_017011103.2:c.4662C>G	XP_016866592.1:p.Asn1554Lys
XM_017011104.1:c.4632C>G	XP_016866593.1:p.Asn1544Lys
XM_017011105.2:c.4602C>G	XP_016866594.1:p.Asn1534Lys
XM_017011106.2:c.4473C>G	XP_016866595.1:p.Asn1491Lys
XM_017011107.2:c.4452C>G	XP_016866596.1:p.Asn1484Lys
XR_002956289.1:n.4747C>G
NM_001363725.2:c.2301C>G	NP_001350654.1:p.Asn767Lys
NM_001371656.1:c.4680C>G	NP_001358585.1:p.Asn1560Lys
NM_001374820.1:c.4680C>G	NP_001361749.1:p.Asn1560Lys
NM_001374828.1:c.4800C>G MANE Select	NP_001361757.1:p.Asn1600Lys
NM_017519.3:c.4641C>G	NP_059989.3:p.Asn1547Lys