Canonical Allele Identifier: CA366241602

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522164A>G (hg19) ; chr6:g.157201030A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201030A>G , CM000668.2:g.157201030A>G	GRCh38
NC_000006.11:g.157522164A>G , CM000668.1:g.157522164A>G	GRCh37
NC_000006.10:g.157563856A>G	NCBI36
NG_032093.1:g.428101A>G
NG_032093.2:g.428101A>G
NG_066624.1:g.430005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4646A>G	ENSP00000055163.8:p.Gln1549Arg
ENST00000414678.8:c.4715A>G	ENSP00000412835.3:p.Gln1572Arg
ENST00000637015.2:c.4934A>G	ENSP00000489729.2:p.Gln1645Arg
ENST00000346085.10:c.4685A>G	ENSP00000344546.5:p.Gln1562Arg
ENST00000350026.10:c.4397A>G	ENSP00000055163.7:p.Gln1466Arg
ENST00000414678.7:c.2963A>G	ENSP00000412835.2:p.Gln988Arg
ENST00000635849.1:c.2126A>G	ENSP00000490948.1:p.Gln709Arg
ENST00000635957.1:c.1757A>G	ENSP00000490385.1:p.Gln586Arg
ENST00000636227.1:n.3268A>G
ENST00000636254.1:n.725A>G
ENST00000636930.2:c.4805A>G MANE Select	ENSP00000490491.2:p.Gln1602Arg
ENST00000636940.1:n.2802A>G
ENST00000637015.1:c.2173A>G
ENST00000637568.1:c.2087A>G
ENST00000637741.1:n.1471A>G
ENST00000637810.1:c.2147A>G	ENSP00000489636.1:p.Gln716Arg
ENST00000637904.1:c.2306A>G	ENSP00000490550.1:p.Gln769Arg
ENST00000647938.1:c.4436A>G	ENSP00000498155.1:p.Gln1479Arg
ENST00000346085.9:c.4436A>G	ENSP00000344546.4:p.Gln1479Arg
ENST00000350026.9:c.4397A>G	ENSP00000055163.7:p.Gln1466Arg
ENST00000414678.6:c.2963A>G	ENSP00000412835.2:p.Gln988Arg
NM_017519.2:c.4397A>G	NP_059989.2:p.Gln1466Arg
NM_020732.3:c.4436A>G	NP_065783.3:p.Gln1479Arg
XM_005267069.3:c.4556A>G	XP_005267126.2:p.Gln1519Arg
XM_011535984.1:c.3635A>G	XP_011534286.1:p.Gln1212Arg
XM_011535985.1:c.3455A>G	XP_011534287.1:p.Gln1152Arg
XM_011535986.1:c.3215A>G	XP_011534288.1:p.Gln1072Arg
XM_011535987.1:c.2834A>G	XP_011534289.1:p.Gln945Arg
XM_011535988.1:c.1697A>G	XP_011534290.1:p.Gln566Arg
NM_001346813.1:c.4556A>G	NP_001333742.1:p.Gln1519Arg
NM_001363725.1:c.2306A>G	NP_001350654.1:p.Gln769Arg
XM_011535984.2:c.4766A>G	XP_011534286.2:p.Gln1589Arg
XM_011535988.3:c.1697A>G	XP_011534290.1:p.Gln566Arg
XM_017011103.2:c.4667A>G	XP_016866592.1:p.Gln1556Arg
XM_017011104.1:c.4637A>G	XP_016866593.1:p.Gln1546Arg
XM_017011105.2:c.4607A>G	XP_016866594.1:p.Gln1536Arg
XM_017011106.2:c.4478A>G	XP_016866595.1:p.Gln1493Arg
XM_017011107.2:c.4457A>G	XP_016866596.1:p.Gln1486Arg
XR_002956289.1:n.4752A>G
NM_001363725.2:c.2306A>G	NP_001350654.1:p.Gln769Arg
NM_001371656.1:c.4685A>G	NP_001358585.1:p.Gln1562Arg
NM_001374820.1:c.4685A>G	NP_001361749.1:p.Gln1562Arg
NM_001374828.1:c.4805A>G MANE Select	NP_001361757.1:p.Gln1602Arg
NM_017519.3:c.4646A>G	NP_059989.3:p.Gln1549Arg