Canonical Allele Identifier: CA366234222

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510885C>G (hg19) ; chr6:g.157189751C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189751C>G , CM000668.2:g.157189751C>G	GRCh38
NC_000006.11:g.157510885C>G , CM000668.1:g.157510885C>G	GRCh37
NC_000006.10:g.157552577C>G	NCBI36
NG_032093.1:g.416822C>G
NG_032093.2:g.416822C>G
NG_066624.1:g.418726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3870C>G	ENSP00000055163.8:p.His1290Gln
ENST00000414678.8:c.3939C>G	ENSP00000412835.3:p.His1313Gln
ENST00000637015.2:c.4158C>G	ENSP00000489729.2:p.His1386Gln
ENST00000346085.10:c.3909C>G	ENSP00000344546.5:p.His1303Gln
ENST00000350026.10:c.3621C>G	ENSP00000055163.7:p.His1207Gln
ENST00000414678.7:c.2187C>G	ENSP00000412835.2:p.His729Gln
ENST00000635849.1:c.1350C>G	ENSP00000490948.1:p.His450Gln
ENST00000635957.1:c.984C>G	ENSP00000490385.1:p.His328Gln
ENST00000636930.2:c.4029C>G MANE Select	ENSP00000490491.2:p.His1343Gln
ENST00000636940.1:n.2026C>G
ENST00000637015.1:c.1397C>G
ENST00000637568.1:c.1311C>G
ENST00000637741.1:n.695C>G
ENST00000637810.1:c.1371C>G	ENSP00000489636.1:p.His457Gln
ENST00000637904.1:c.1530C>G	ENSP00000490550.1:p.His510Gln
ENST00000647938.1:c.3660C>G	ENSP00000498155.1:p.His1220Gln
ENST00000346085.9:c.3660C>G	ENSP00000344546.4:p.His1220Gln
ENST00000350026.9:c.3621C>G	ENSP00000055163.7:p.His1207Gln
ENST00000414678.6:c.2187C>G	ENSP00000412835.2:p.His729Gln
NM_017519.2:c.3621C>G	NP_059989.2:p.His1207Gln
NM_020732.3:c.3660C>G	NP_065783.3:p.His1220Gln
XM_005267069.3:c.3780C>G	XP_005267126.2:p.His1260Gln
XM_011535984.1:c.2859C>G	XP_011534286.1:p.His953Gln
XM_011535985.1:c.2679C>G	XP_011534287.1:p.His893Gln
XM_011535986.1:c.2439C>G	XP_011534288.1:p.His813Gln
XM_011535987.1:c.2058C>G	XP_011534289.1:p.His686Gln
XM_011535988.1:c.921C>G	XP_011534290.1:p.His307Gln
NM_001346813.1:c.3780C>G	NP_001333742.1:p.His1260Gln
NM_001363725.1:c.1530C>G	NP_001350654.1:p.His510Gln
XM_011535984.2:c.3990C>G	XP_011534286.2:p.His1330Gln
XM_011535988.3:c.921C>G	XP_011534290.1:p.His307Gln
XM_017011103.2:c.3891C>G	XP_016866592.1:p.His1297Gln
XM_017011104.1:c.3861C>G	XP_016866593.1:p.His1287Gln
XM_017011105.2:c.3831C>G	XP_016866594.1:p.His1277Gln
XM_017011106.2:c.3702C>G	XP_016866595.1:p.His1234Gln
XM_017011107.2:c.3681C>G	XP_016866596.1:p.His1227Gln
XR_002956289.1:n.4073C>G
NM_001363725.2:c.1530C>G	NP_001350654.1:p.His510Gln
NM_001371656.1:c.3909C>G	NP_001358585.1:p.His1303Gln
NM_001374820.1:c.3909C>G	NP_001361749.1:p.His1303Gln
NM_001374828.1:c.4029C>G MANE Select	NP_001361757.1:p.His1343Gln
NM_017519.3:c.3870C>G	NP_059989.3:p.His1290Gln