Canonical Allele Identifier: CA366242342

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522389C>G (hg19) ; chr6:g.157201255C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201255C>G , CM000668.2:g.157201255C>G	GRCh38
NC_000006.11:g.157522389C>G , CM000668.1:g.157522389C>G	GRCh37
NC_000006.10:g.157564081C>G	NCBI36
NG_032093.1:g.428326C>G
NG_032093.2:g.428326C>G
NG_066624.1:g.430230C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4871C>G	ENSP00000055163.8:p.Pro1624Arg
ENST00000414678.8:c.4940C>G	ENSP00000412835.3:p.Pro1647Arg
ENST00000637015.2:c.5159C>G	ENSP00000489729.2:p.Pro1720Arg
ENST00000346085.10:c.4910C>G	ENSP00000344546.5:p.Pro1637Arg
ENST00000350026.10:c.4622C>G	ENSP00000055163.7:p.Pro1541Arg
ENST00000414678.7:c.3188C>G	ENSP00000412835.2:p.Pro1063Arg
ENST00000635849.1:c.2351C>G	ENSP00000490948.1:p.Pro784Arg
ENST00000635957.1:c.1982C>G	ENSP00000490385.1:p.Pro661Arg
ENST00000636227.1:n.3493C>G
ENST00000636254.1:n.950C>G
ENST00000636930.2:c.5030C>G MANE Select	ENSP00000490491.2:p.Pro1677Arg
ENST00000636940.1:n.3027C>G
ENST00000637015.1:c.2398C>G
ENST00000637568.1:c.2312C>G
ENST00000637741.1:n.1696C>G
ENST00000637810.1:c.2372C>G	ENSP00000489636.1:p.Pro791Arg
ENST00000637904.1:c.2531C>G	ENSP00000490550.1:p.Pro844Arg
ENST00000647938.1:c.4661C>G	ENSP00000498155.1:p.Pro1554Arg
ENST00000346085.9:c.4661C>G	ENSP00000344546.4:p.Pro1554Arg
ENST00000350026.9:c.4622C>G	ENSP00000055163.7:p.Pro1541Arg
ENST00000414678.6:c.3188C>G	ENSP00000412835.2:p.Pro1063Arg
NM_017519.2:c.4622C>G	NP_059989.2:p.Pro1541Arg
NM_020732.3:c.4661C>G	NP_065783.3:p.Pro1554Arg
XM_005267069.3:c.4781C>G	XP_005267126.2:p.Pro1594Arg
XM_011535984.1:c.3860C>G	XP_011534286.1:p.Pro1287Arg
XM_011535985.1:c.3680C>G	XP_011534287.1:p.Pro1227Arg
XM_011535986.1:c.3440C>G	XP_011534288.1:p.Pro1147Arg
XM_011535987.1:c.3059C>G	XP_011534289.1:p.Pro1020Arg
XM_011535988.1:c.1922C>G	XP_011534290.1:p.Pro641Arg
NM_001346813.1:c.4781C>G	NP_001333742.1:p.Pro1594Arg
NM_001363725.1:c.2531C>G	NP_001350654.1:p.Pro844Arg
XM_011535984.2:c.4991C>G	XP_011534286.2:p.Pro1664Arg
XM_011535988.3:c.1922C>G	XP_011534290.1:p.Pro641Arg
XM_017011103.2:c.4892C>G	XP_016866592.1:p.Pro1631Arg
XM_017011104.1:c.4862C>G	XP_016866593.1:p.Pro1621Arg
XM_017011105.2:c.4832C>G	XP_016866594.1:p.Pro1611Arg
XM_017011106.2:c.4703C>G	XP_016866595.1:p.Pro1568Arg
XM_017011107.2:c.4682C>G	XP_016866596.1:p.Pro1561Arg
XR_002956289.1:n.4977C>G
NM_001363725.2:c.2531C>G	NP_001350654.1:p.Pro844Arg
NM_001371656.1:c.4910C>G	NP_001358585.1:p.Pro1637Arg
NM_001374820.1:c.4910C>G	NP_001361749.1:p.Pro1637Arg
NM_001374828.1:c.5030C>G MANE Select	NP_001361757.1:p.Pro1677Arg
NM_017519.3:c.4871C>G	NP_059989.3:p.Pro1624Arg