Canonical Allele Identifier: CA366242475

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522446C>A (hg19) ; chr6:g.157201312C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201312C>A , CM000668.2:g.157201312C>A	GRCh38
NC_000006.11:g.157522446C>A , CM000668.1:g.157522446C>A	GRCh37
NC_000006.10:g.157564138C>A	NCBI36
NG_032093.1:g.428383C>A
NG_032093.2:g.428383C>A
NG_066624.1:g.430287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4928C>A	ENSP00000055163.8:p.Pro1643His
ENST00000414678.8:c.4997C>A	ENSP00000412835.3:p.Pro1666His
ENST00000637015.2:c.5216C>A	ENSP00000489729.2:p.Pro1739His
ENST00000346085.10:c.4967C>A	ENSP00000344546.5:p.Pro1656His
ENST00000350026.10:c.4679C>A	ENSP00000055163.7:p.Pro1560His
ENST00000414678.7:c.3245C>A	ENSP00000412835.2:p.Pro1082His
ENST00000635849.1:c.2408C>A	ENSP00000490948.1:p.Pro803His
ENST00000635957.1:c.2039C>A	ENSP00000490385.1:p.Pro680His
ENST00000636227.1:n.3550C>A
ENST00000636254.1:n.1007C>A
ENST00000636930.2:c.5087C>A MANE Select	ENSP00000490491.2:p.Pro1696His
ENST00000636940.1:n.3084C>A
ENST00000637015.1:c.2455C>A
ENST00000637568.1:c.2369C>A
ENST00000637741.1:n.1753C>A
ENST00000637810.1:c.2429C>A	ENSP00000489636.1:p.Pro810His
ENST00000637904.1:c.2588C>A	ENSP00000490550.1:p.Pro863His
ENST00000647938.1:c.4718C>A	ENSP00000498155.1:p.Pro1573His
ENST00000346085.9:c.4718C>A	ENSP00000344546.4:p.Pro1573His
ENST00000350026.9:c.4679C>A	ENSP00000055163.7:p.Pro1560His
ENST00000414678.6:c.3245C>A	ENSP00000412835.2:p.Pro1082His
NM_017519.2:c.4679C>A	NP_059989.2:p.Pro1560His
NM_020732.3:c.4718C>A	NP_065783.3:p.Pro1573His
XM_005267069.3:c.4838C>A	XP_005267126.2:p.Pro1613His
XM_011535984.1:c.3917C>A	XP_011534286.1:p.Pro1306His
XM_011535985.1:c.3737C>A	XP_011534287.1:p.Pro1246His
XM_011535986.1:c.3497C>A	XP_011534288.1:p.Pro1166His
XM_011535987.1:c.3116C>A	XP_011534289.1:p.Pro1039His
XM_011535988.1:c.1979C>A	XP_011534290.1:p.Pro660His
NM_001346813.1:c.4838C>A	NP_001333742.1:p.Pro1613His
NM_001363725.1:c.2588C>A	NP_001350654.1:p.Pro863His
XM_011535984.2:c.5048C>A	XP_011534286.2:p.Pro1683His
XM_011535988.3:c.1979C>A	XP_011534290.1:p.Pro660His
XM_017011103.2:c.4949C>A	XP_016866592.1:p.Pro1650His
XM_017011104.1:c.4919C>A	XP_016866593.1:p.Pro1640His
XM_017011105.2:c.4889C>A	XP_016866594.1:p.Pro1630His
XM_017011106.2:c.4760C>A	XP_016866595.1:p.Pro1587His
XM_017011107.2:c.4739C>A	XP_016866596.1:p.Pro1580His
XR_002956289.1:n.5034C>A
NM_001363725.2:c.2588C>A	NP_001350654.1:p.Pro863His
NM_001371656.1:c.4967C>A	NP_001358585.1:p.Pro1656His
NM_001374820.1:c.4967C>A	NP_001361749.1:p.Pro1656His
NM_001374828.1:c.5087C>A MANE Select	NP_001361757.1:p.Pro1696His
NM_017519.3:c.4928C>A	NP_059989.3:p.Pro1643His