Canonical Allele Identifier: CA366388640

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469776C>G (hg19) ; chr6:g.157148642C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148642C>G , CM000668.2:g.157148642C>G	GRCh38
NC_000006.11:g.157469776C>G , CM000668.1:g.157469776C>G	GRCh37
NC_000006.10:g.157511468C>G	NCBI36
NG_032093.1:g.375713C>G
NG_032093.2:g.375713C>G
NG_066624.1:g.377617C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2780C>G	ENSP00000055163.8:p.Pro927Arg
ENST00000414678.8:c.2690C>G	ENSP00000412835.3:p.Pro897Arg
ENST00000637015.2:c.2780C>G	ENSP00000489729.2:p.Pro927Arg
ENST00000319584.11:c.794C>G	ENSP00000313006.7:p.Pro265Arg
ENST00000346085.10:c.2819C>G	ENSP00000344546.5:p.Pro940Arg
ENST00000350026.10:c.2531C>G	ENSP00000055163.7:p.Pro844Arg
ENST00000414678.7:c.938C>G	ENSP00000412835.2:p.Pro313Arg
ENST00000452544.2:n.681C>G
ENST00000635849.1:c.101C>G	ENSP00000490948.1:p.Pro34Arg
ENST00000636930.2:c.2780C>G MANE Select	ENSP00000490491.2:p.Pro927Arg
ENST00000637015.1:c.19C>G
ENST00000637810.1:c.281C>G	ENSP00000489636.1:p.Pro94Arg
ENST00000637904.1:c.281C>G	ENSP00000490550.1:p.Pro94Arg
ENST00000647938.1:c.2570C>G	ENSP00000498155.1:p.Pro857Arg
ENST00000674190.1:n.1529C>G
ENST00000319584.10:c.797C>G	ENSP00000313006.6:p.Pro266Arg
ENST00000346085.9:c.2570C>G	ENSP00000344546.4:p.Pro857Arg
ENST00000350026.9:c.2531C>G	ENSP00000055163.7:p.Pro844Arg
ENST00000414678.6:c.938C>G	ENSP00000412835.2:p.Pro313Arg
ENST00000452544.1:n.627C>G
NM_017519.2:c.2531C>G	NP_059989.2:p.Pro844Arg
NM_020732.3:c.2570C>G	NP_065783.3:p.Pro857Arg
XM_005267069.3:c.2531C>G	XP_005267126.2:p.Pro844Arg
XM_011535984.1:c.1481C>G	XP_011534286.1:p.Pro494Arg
XM_011535985.1:c.1301C>G	XP_011534287.1:p.Pro434Arg
XM_011535986.1:c.1061C>G	XP_011534288.1:p.Pro354Arg
XM_011535987.1:c.680C>G	XP_011534289.1:p.Pro227Arg
XM_011535988.1:c.-20+15435C>G	XP_011534290.1:n.-20+15435C>G
NM_001346813.1:c.2531C>G	NP_001333742.1:p.Pro844Arg
NM_001363725.1:c.281C>G	NP_001350654.1:p.Pro94Arg
XM_011535984.2:c.2612C>G	XP_011534286.2:p.Pro871Arg
XM_011535988.3:c.-20+15435C>G	XP_011534290.1:n.-20+15435C>G
XM_017011103.2:c.2612C>G	XP_016866592.1:p.Pro871Arg
XM_017011104.1:c.2612C>G	XP_016866593.1:p.Pro871Arg
XM_017011105.2:c.2612C>G	XP_016866594.1:p.Pro871Arg
XM_017011106.2:c.2612C>G	XP_016866595.1:p.Pro871Arg
XM_017011107.2:c.2432C>G	XP_016866596.1:p.Pro811Arg
XR_002956289.1:n.2695C>G
NM_001363725.2:c.281C>G	NP_001350654.1:p.Pro94Arg
NM_001371656.1:c.2819C>G	NP_001358585.1:p.Pro940Arg
NM_001374820.1:c.2819C>G	NP_001361749.1:p.Pro940Arg
NM_001374828.1:c.2780C>G MANE Select	NP_001361757.1:p.Pro927Arg
NM_017519.3:c.2780C>G	NP_059989.3:p.Pro927Arg