Canonical Allele Identifier: CA366389021

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469951C>G (hg19) ; chr6:g.157148817C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148817C>G , CM000668.2:g.157148817C>G	GRCh38
NC_000006.11:g.157469951C>G , CM000668.1:g.157469951C>G	GRCh37
NC_000006.10:g.157511643C>G	NCBI36
NG_032093.1:g.375888C>G
NG_032093.2:g.375888C>G
NG_066624.1:g.377792C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2955C>G	ENSP00000055163.8:p.Ser985Arg
ENST00000414678.8:c.2865C>G	ENSP00000412835.3:p.Ser955Arg
ENST00000637015.2:c.2955C>G	ENSP00000489729.2:p.Ser985Arg
ENST00000319584.11:c.969C>G	ENSP00000313006.7:p.Ser323Arg
ENST00000346085.10:c.2994C>G	ENSP00000344546.5:p.Ser998Arg
ENST00000350026.10:c.2706C>G	ENSP00000055163.7:p.Ser902Arg
ENST00000414678.7:c.1113C>G	ENSP00000412835.2:p.Ser371Arg
ENST00000452544.2:n.856C>G
ENST00000635849.1:c.276C>G	ENSP00000490948.1:p.Ser92Arg
ENST00000636426.1:n.89C>G
ENST00000636930.2:c.2955C>G MANE Select	ENSP00000490491.2:p.Ser985Arg
ENST00000637015.1:c.194C>G
ENST00000637810.1:c.456C>G	ENSP00000489636.1:p.Ser152Arg
ENST00000637904.1:c.456C>G	ENSP00000490550.1:p.Ser152Arg
ENST00000647938.1:c.2745C>G	ENSP00000498155.1:p.Ser915Arg
ENST00000674190.1:n.1704C>G
ENST00000319584.10:c.972C>G	ENSP00000313006.6:p.Ser324Arg
ENST00000346085.9:c.2745C>G	ENSP00000344546.4:p.Ser915Arg
ENST00000350026.9:c.2706C>G	ENSP00000055163.7:p.Ser902Arg
ENST00000414678.6:c.1113C>G	ENSP00000412835.2:p.Ser371Arg
ENST00000452544.1:n.802C>G
ENST00000478761.3:c.28C>G
NM_017519.2:c.2706C>G	NP_059989.2:p.Ser902Arg
NM_020732.3:c.2745C>G	NP_065783.3:p.Ser915Arg
XM_005267069.3:c.2706C>G	XP_005267126.2:p.Ser902Arg
XM_011535984.1:c.1656C>G	XP_011534286.1:p.Ser552Arg
XM_011535985.1:c.1476C>G	XP_011534287.1:p.Ser492Arg
XM_011535986.1:c.1236C>G	XP_011534288.1:p.Ser412Arg
XM_011535987.1:c.855C>G	XP_011534289.1:p.Ser285Arg
XM_011535988.1:c.-20+15610C>G	XP_011534290.1:n.-20+15610C>G
NM_001346813.1:c.2706C>G	NP_001333742.1:p.Ser902Arg
NM_001363725.1:c.456C>G	NP_001350654.1:p.Ser152Arg
XM_011535984.2:c.2787C>G	XP_011534286.2:p.Ser929Arg
XM_011535988.3:c.-20+15610C>G	XP_011534290.1:n.-20+15610C>G
XM_017011103.2:c.2787C>G	XP_016866592.1:p.Ser929Arg
XM_017011104.1:c.2787C>G	XP_016866593.1:p.Ser929Arg
XM_017011105.2:c.2787C>G	XP_016866594.1:p.Ser929Arg
XM_017011106.2:c.2787C>G	XP_016866595.1:p.Ser929Arg
XM_017011107.2:c.2607C>G	XP_016866596.1:p.Ser869Arg
XR_002956289.1:n.2870C>G
NM_001363725.2:c.456C>G	NP_001350654.1:p.Ser152Arg
NM_001371656.1:c.2994C>G	NP_001358585.1:p.Ser998Arg
NM_001374820.1:c.2994C>G	NP_001361749.1:p.Ser998Arg
NM_001374828.1:c.2955C>G MANE Select	NP_001361757.1:p.Ser985Arg
NM_017519.3:c.2955C>G	NP_059989.3:p.Ser985Arg