Canonical Allele Identifier: CA366241791

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4682C>A	ENSP00000055163.8:p.Pro1561Gln
ENST00000414678.8:c.4751C>A	ENSP00000412835.3:p.Pro1584Gln
ENST00000637015.2:c.4970C>A	ENSP00000489729.2:p.Pro1657Gln
ENST00000346085.10:c.4721C>A	ENSP00000344546.5:p.Pro1574Gln
ENST00000350026.10:c.4433C>A	ENSP00000055163.7:p.Pro1478Gln
ENST00000414678.7:c.2999C>A	ENSP00000412835.2:p.Pro1000Gln
ENST00000635849.1:c.2162C>A	ENSP00000490948.1:p.Pro721Gln
ENST00000635957.1:c.1793C>A	ENSP00000490385.1:p.Pro598Gln
ENST00000636227.1:n.3304C>A
ENST00000636254.1:n.761C>A
ENST00000636930.2:c.4841C>A MANE Select	ENSP00000490491.2:p.Pro1614Gln
ENST00000636940.1:n.2838C>A
ENST00000637015.1:c.2209C>A
ENST00000637568.1:c.2123C>A
ENST00000637741.1:n.1507C>A
ENST00000637810.1:c.2183C>A	ENSP00000489636.1:p.Pro728Gln
ENST00000637904.1:c.2342C>A	ENSP00000490550.1:p.Pro781Gln
ENST00000647938.1:c.4472C>A	ENSP00000498155.1:p.Pro1491Gln
ENST00000346085.9:c.4472C>A	ENSP00000344546.4:p.Pro1491Gln
ENST00000350026.9:c.4433C>A	ENSP00000055163.7:p.Pro1478Gln
ENST00000414678.6:c.2999C>A	ENSP00000412835.2:p.Pro1000Gln
NM_017519.2:c.4433C>A	NP_059989.2:p.Pro1478Gln
NM_020732.3:c.4472C>A	NP_065783.3:p.Pro1491Gln
XM_005267069.3:c.4592C>A	XP_005267126.2:p.Pro1531Gln
XM_011535984.1:c.3671C>A	XP_011534286.1:p.Pro1224Gln
XM_011535985.1:c.3491C>A	XP_011534287.1:p.Pro1164Gln
XM_011535986.1:c.3251C>A	XP_011534288.1:p.Pro1084Gln
XM_011535987.1:c.2870C>A	XP_011534289.1:p.Pro957Gln
XM_011535988.1:c.1733C>A	XP_011534290.1:p.Pro578Gln
NM_001346813.1:c.4592C>A	NP_001333742.1:p.Pro1531Gln
NM_001363725.1:c.2342C>A	NP_001350654.1:p.Pro781Gln
XM_011535984.2:c.4802C>A	XP_011534286.2:p.Pro1601Gln
XM_011535988.3:c.1733C>A	XP_011534290.1:p.Pro578Gln
XM_017011103.2:c.4703C>A	XP_016866592.1:p.Pro1568Gln
XM_017011104.1:c.4673C>A	XP_016866593.1:p.Pro1558Gln
XM_017011105.2:c.4643C>A	XP_016866594.1:p.Pro1548Gln
XM_017011106.2:c.4514C>A	XP_016866595.1:p.Pro1505Gln
XM_017011107.2:c.4493C>A	XP_016866596.1:p.Pro1498Gln
XR_002956289.1:n.4788C>A
NM_001363725.2:c.2342C>A	NP_001350654.1:p.Pro781Gln
NM_001371656.1:c.4721C>A	NP_001358585.1:p.Pro1574Gln
NM_001374820.1:c.4721C>A	NP_001361749.1:p.Pro1574Gln
NM_001374828.1:c.4841C>A MANE Select	NP_001361757.1:p.Pro1614Gln
NM_017519.3:c.4682C>A	NP_059989.3:p.Pro1561Gln