Canonical Allele Identifier: CA366242297

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522368C>G (hg19) ; chr6:g.157201234C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201234C>G , CM000668.2:g.157201234C>G	GRCh38
NC_000006.11:g.157522368C>G , CM000668.1:g.157522368C>G	GRCh37
NC_000006.10:g.157564060C>G	NCBI36
NG_032093.1:g.428305C>G
NG_032093.2:g.428305C>G
NG_066624.1:g.430209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4850C>G	ENSP00000055163.8:p.Pro1617Arg
ENST00000414678.8:c.4919C>G	ENSP00000412835.3:p.Pro1640Arg
ENST00000637015.2:c.5138C>G	ENSP00000489729.2:p.Pro1713Arg
ENST00000346085.10:c.4889C>G	ENSP00000344546.5:p.Pro1630Arg
ENST00000350026.10:c.4601C>G	ENSP00000055163.7:p.Pro1534Arg
ENST00000414678.7:c.3167C>G	ENSP00000412835.2:p.Pro1056Arg
ENST00000635849.1:c.2330C>G	ENSP00000490948.1:p.Pro777Arg
ENST00000635957.1:c.1961C>G	ENSP00000490385.1:p.Pro654Arg
ENST00000636227.1:n.3472C>G
ENST00000636254.1:n.929C>G
ENST00000636930.2:c.5009C>G MANE Select	ENSP00000490491.2:p.Pro1670Arg
ENST00000636940.1:n.3006C>G
ENST00000637015.1:c.2377C>G
ENST00000637568.1:c.2291C>G
ENST00000637741.1:n.1675C>G
ENST00000637810.1:c.2351C>G	ENSP00000489636.1:p.Pro784Arg
ENST00000637904.1:c.2510C>G	ENSP00000490550.1:p.Pro837Arg
ENST00000647938.1:c.4640C>G	ENSP00000498155.1:p.Pro1547Arg
ENST00000346085.9:c.4640C>G	ENSP00000344546.4:p.Pro1547Arg
ENST00000350026.9:c.4601C>G	ENSP00000055163.7:p.Pro1534Arg
ENST00000414678.6:c.3167C>G	ENSP00000412835.2:p.Pro1056Arg
NM_017519.2:c.4601C>G	NP_059989.2:p.Pro1534Arg
NM_020732.3:c.4640C>G	NP_065783.3:p.Pro1547Arg
XM_005267069.3:c.4760C>G	XP_005267126.2:p.Pro1587Arg
XM_011535984.1:c.3839C>G	XP_011534286.1:p.Pro1280Arg
XM_011535985.1:c.3659C>G	XP_011534287.1:p.Pro1220Arg
XM_011535986.1:c.3419C>G	XP_011534288.1:p.Pro1140Arg
XM_011535987.1:c.3038C>G	XP_011534289.1:p.Pro1013Arg
XM_011535988.1:c.1901C>G	XP_011534290.1:p.Pro634Arg
NM_001346813.1:c.4760C>G	NP_001333742.1:p.Pro1587Arg
NM_001363725.1:c.2510C>G	NP_001350654.1:p.Pro837Arg
XM_011535984.2:c.4970C>G	XP_011534286.2:p.Pro1657Arg
XM_011535988.3:c.1901C>G	XP_011534290.1:p.Pro634Arg
XM_017011103.2:c.4871C>G	XP_016866592.1:p.Pro1624Arg
XM_017011104.1:c.4841C>G	XP_016866593.1:p.Pro1614Arg
XM_017011105.2:c.4811C>G	XP_016866594.1:p.Pro1604Arg
XM_017011106.2:c.4682C>G	XP_016866595.1:p.Pro1561Arg
XM_017011107.2:c.4661C>G	XP_016866596.1:p.Pro1554Arg
XR_002956289.1:n.4956C>G
NM_001363725.2:c.2510C>G	NP_001350654.1:p.Pro837Arg
NM_001371656.1:c.4889C>G	NP_001358585.1:p.Pro1630Arg
NM_001374820.1:c.4889C>G	NP_001361749.1:p.Pro1630Arg
NM_001374828.1:c.5009C>G MANE Select	NP_001361757.1:p.Pro1670Arg
NM_017519.3:c.4850C>G	NP_059989.3:p.Pro1617Arg