Canonical Allele Identifier: CA366239655

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519976C>A (hg19) ; chr6:g.157198842C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198842C>A , CM000668.2:g.157198842C>A	GRCh38
NC_000006.11:g.157519976C>A , CM000668.1:g.157519976C>A	GRCh37
NC_000006.10:g.157561668C>A	NCBI36
NG_032093.1:g.425913C>A
NG_032093.2:g.425913C>A
NG_066624.1:g.427817C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4255C>A	ENSP00000055163.8:p.Gln1419Lys
ENST00000414678.8:c.4324C>A	ENSP00000412835.3:p.Gln1442Lys
ENST00000637015.2:c.4543C>A	ENSP00000489729.2:p.Gln1515Lys
ENST00000346085.10:c.4294C>A	ENSP00000344546.5:p.Gln1432Lys
ENST00000350026.10:c.4006C>A	ENSP00000055163.7:p.Gln1336Lys
ENST00000414678.7:c.2572C>A	ENSP00000412835.2:p.Gln858Lys
ENST00000635849.1:c.1735C>A	ENSP00000490948.1:p.Gln579Lys
ENST00000635957.1:c.1366C>A	ENSP00000490385.1:p.Gln456Lys
ENST00000636227.1:n.2877C>A
ENST00000636254.1:n.334C>A
ENST00000636930.2:c.4414C>A MANE Select	ENSP00000490491.2:p.Gln1472Lys
ENST00000636940.1:n.2411C>A
ENST00000637015.1:c.1782C>A
ENST00000637568.1:c.1696C>A
ENST00000637741.1:n.1080C>A
ENST00000637810.1:c.1756C>A	ENSP00000489636.1:p.Gln586Lys
ENST00000637904.1:c.1915C>A	ENSP00000490550.1:p.Gln639Lys
ENST00000647938.1:c.4045C>A	ENSP00000498155.1:p.Gln1349Lys
ENST00000346085.9:c.4045C>A	ENSP00000344546.4:p.Gln1349Lys
ENST00000350026.9:c.4006C>A	ENSP00000055163.7:p.Gln1336Lys
ENST00000414678.6:c.2572C>A	ENSP00000412835.2:p.Gln858Lys
NM_017519.2:c.4006C>A	NP_059989.2:p.Gln1336Lys
NM_020732.3:c.4045C>A	NP_065783.3:p.Gln1349Lys
XM_005267069.3:c.4165C>A	XP_005267126.2:p.Gln1389Lys
XM_011535984.1:c.3244C>A	XP_011534286.1:p.Gln1082Lys
XM_011535985.1:c.3064C>A	XP_011534287.1:p.Gln1022Lys
XM_011535986.1:c.2824C>A	XP_011534288.1:p.Gln942Lys
XM_011535987.1:c.2443C>A	XP_011534289.1:p.Gln815Lys
XM_011535988.1:c.1306C>A	XP_011534290.1:p.Gln436Lys
NM_001346813.1:c.4165C>A	NP_001333742.1:p.Gln1389Lys
NM_001363725.1:c.1915C>A	NP_001350654.1:p.Gln639Lys
XM_011535984.2:c.4375C>A	XP_011534286.2:p.Gln1459Lys
XM_011535988.3:c.1306C>A	XP_011534290.1:p.Gln436Lys
XM_017011103.2:c.4276C>A	XP_016866592.1:p.Gln1426Lys
XM_017011104.1:c.4246C>A	XP_016866593.1:p.Gln1416Lys
XM_017011105.2:c.4216C>A	XP_016866594.1:p.Gln1406Lys
XM_017011106.2:c.4087C>A	XP_016866595.1:p.Gln1363Lys
XM_017011107.2:c.4066C>A	XP_016866596.1:p.Gln1356Lys
XR_002956289.1:n.4427-1863C>A
NM_001363725.2:c.1915C>A	NP_001350654.1:p.Gln639Lys
NM_001371656.1:c.4294C>A	NP_001358585.1:p.Gln1432Lys
NM_001374820.1:c.4294C>A	NP_001361749.1:p.Gln1432Lys
NM_001374828.1:c.4414C>A MANE Select	NP_001361757.1:p.Gln1472Lys
NM_017519.3:c.4255C>A	NP_059989.3:p.Gln1419Lys