Canonical Allele Identifier: CA366234123

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510836C>T (hg19) ; chr6:g.157189702C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189702C>T , CM000668.2:g.157189702C>T	GRCh38
NC_000006.11:g.157510836C>T , CM000668.1:g.157510836C>T	GRCh37
NC_000006.10:g.157552528C>T	NCBI36
NG_032093.1:g.416773C>T
NG_032093.2:g.416773C>T
NG_066624.1:g.418677C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3821C>T	ENSP00000055163.8:p.Ala1274Val
ENST00000414678.8:c.3890C>T	ENSP00000412835.3:p.Ala1297Val
ENST00000637015.2:c.4109C>T	ENSP00000489729.2:p.Ala1370Val
ENST00000346085.10:c.3860C>T	ENSP00000344546.5:p.Ala1287Val
ENST00000350026.10:c.3572C>T	ENSP00000055163.7:p.Ala1191Val
ENST00000414678.7:c.2138C>T	ENSP00000412835.2:p.Ala713Val
ENST00000635849.1:c.1301C>T	ENSP00000490948.1:p.Ala434Val
ENST00000635957.1:c.935C>T	ENSP00000490385.1:p.Ala312Val
ENST00000636930.2:c.3980C>T MANE Select	ENSP00000490491.2:p.Ala1327Val
ENST00000636940.1:n.1977C>T
ENST00000637015.1:c.1348C>T
ENST00000637568.1:c.1262C>T
ENST00000637741.1:n.646C>T
ENST00000637810.1:c.1322C>T	ENSP00000489636.1:p.Ala441Val
ENST00000637904.1:c.1481C>T	ENSP00000490550.1:p.Ala494Val
ENST00000647938.1:c.3611C>T	ENSP00000498155.1:p.Ala1204Val
ENST00000346085.9:c.3611C>T	ENSP00000344546.4:p.Ala1204Val
ENST00000350026.9:c.3572C>T	ENSP00000055163.7:p.Ala1191Val
ENST00000414678.6:c.2138C>T	ENSP00000412835.2:p.Ala713Val
NM_017519.2:c.3572C>T	NP_059989.2:p.Ala1191Val
NM_020732.3:c.3611C>T	NP_065783.3:p.Ala1204Val
XM_005267069.3:c.3731C>T	XP_005267126.2:p.Ala1244Val
XM_011535984.1:c.2810C>T	XP_011534286.1:p.Ala937Val
XM_011535985.1:c.2630C>T	XP_011534287.1:p.Ala877Val
XM_011535986.1:c.2390C>T	XP_011534288.1:p.Ala797Val
XM_011535987.1:c.2009C>T	XP_011534289.1:p.Ala670Val
XM_011535988.1:c.872C>T	XP_011534290.1:p.Ala291Val
NM_001346813.1:c.3731C>T	NP_001333742.1:p.Ala1244Val
NM_001363725.1:c.1481C>T	NP_001350654.1:p.Ala494Val
XM_011535984.2:c.3941C>T	XP_011534286.2:p.Ala1314Val
XM_011535988.3:c.872C>T	XP_011534290.1:p.Ala291Val
XM_017011103.2:c.3842C>T	XP_016866592.1:p.Ala1281Val
XM_017011104.1:c.3812C>T	XP_016866593.1:p.Ala1271Val
XM_017011105.2:c.3782C>T	XP_016866594.1:p.Ala1261Val
XM_017011106.2:c.3653C>T	XP_016866595.1:p.Ala1218Val
XM_017011107.2:c.3632C>T	XP_016866596.1:p.Ala1211Val
XR_002956289.1:n.4024C>T
NM_001363725.2:c.1481C>T	NP_001350654.1:p.Ala494Val
NM_001371656.1:c.3860C>T	NP_001358585.1:p.Ala1287Val
NM_001374820.1:c.3860C>T	NP_001361749.1:p.Ala1287Val
NM_001374828.1:c.3980C>T MANE Select	NP_001361757.1:p.Ala1327Val
NM_017519.3:c.3821C>T	NP_059989.3:p.Ala1274Val