Canonical Allele Identifier: CA366241793

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522200C>G (hg19) ; chr6:g.157201066C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201066C>G , CM000668.2:g.157201066C>G	GRCh38
NC_000006.11:g.157522200C>G , CM000668.1:g.157522200C>G	GRCh37
NC_000006.10:g.157563892C>G	NCBI36
NG_032093.1:g.428137C>G
NG_032093.2:g.428137C>G
NG_066624.1:g.430041C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4682C>G	ENSP00000055163.8:p.Pro1561Arg
ENST00000414678.8:c.4751C>G	ENSP00000412835.3:p.Pro1584Arg
ENST00000637015.2:c.4970C>G	ENSP00000489729.2:p.Pro1657Arg
ENST00000346085.10:c.4721C>G	ENSP00000344546.5:p.Pro1574Arg
ENST00000350026.10:c.4433C>G	ENSP00000055163.7:p.Pro1478Arg
ENST00000414678.7:c.2999C>G	ENSP00000412835.2:p.Pro1000Arg
ENST00000635849.1:c.2162C>G	ENSP00000490948.1:p.Pro721Arg
ENST00000635957.1:c.1793C>G	ENSP00000490385.1:p.Pro598Arg
ENST00000636227.1:n.3304C>G
ENST00000636254.1:n.761C>G
ENST00000636930.2:c.4841C>G MANE Select	ENSP00000490491.2:p.Pro1614Arg
ENST00000636940.1:n.2838C>G
ENST00000637015.1:c.2209C>G
ENST00000637568.1:c.2123C>G
ENST00000637741.1:n.1507C>G
ENST00000637810.1:c.2183C>G	ENSP00000489636.1:p.Pro728Arg
ENST00000637904.1:c.2342C>G	ENSP00000490550.1:p.Pro781Arg
ENST00000647938.1:c.4472C>G	ENSP00000498155.1:p.Pro1491Arg
ENST00000346085.9:c.4472C>G	ENSP00000344546.4:p.Pro1491Arg
ENST00000350026.9:c.4433C>G	ENSP00000055163.7:p.Pro1478Arg
ENST00000414678.6:c.2999C>G	ENSP00000412835.2:p.Pro1000Arg
NM_017519.2:c.4433C>G	NP_059989.2:p.Pro1478Arg
NM_020732.3:c.4472C>G	NP_065783.3:p.Pro1491Arg
XM_005267069.3:c.4592C>G	XP_005267126.2:p.Pro1531Arg
XM_011535984.1:c.3671C>G	XP_011534286.1:p.Pro1224Arg
XM_011535985.1:c.3491C>G	XP_011534287.1:p.Pro1164Arg
XM_011535986.1:c.3251C>G	XP_011534288.1:p.Pro1084Arg
XM_011535987.1:c.2870C>G	XP_011534289.1:p.Pro957Arg
XM_011535988.1:c.1733C>G	XP_011534290.1:p.Pro578Arg
NM_001346813.1:c.4592C>G	NP_001333742.1:p.Pro1531Arg
NM_001363725.1:c.2342C>G	NP_001350654.1:p.Pro781Arg
XM_011535984.2:c.4802C>G	XP_011534286.2:p.Pro1601Arg
XM_011535988.3:c.1733C>G	XP_011534290.1:p.Pro578Arg
XM_017011103.2:c.4703C>G	XP_016866592.1:p.Pro1568Arg
XM_017011104.1:c.4673C>G	XP_016866593.1:p.Pro1558Arg
XM_017011105.2:c.4643C>G	XP_016866594.1:p.Pro1548Arg
XM_017011106.2:c.4514C>G	XP_016866595.1:p.Pro1505Arg
XM_017011107.2:c.4493C>G	XP_016866596.1:p.Pro1498Arg
XR_002956289.1:n.4788C>G
NM_001363725.2:c.2342C>G	NP_001350654.1:p.Pro781Arg
NM_001371656.1:c.4721C>G	NP_001358585.1:p.Pro1574Arg
NM_001374820.1:c.4721C>G	NP_001361749.1:p.Pro1574Arg
NM_001374828.1:c.4841C>G MANE Select	NP_001361757.1:p.Pro1614Arg
NM_017519.3:c.4682C>G	NP_059989.3:p.Pro1561Arg