Canonical Allele Identifier: CA366242381

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522407A>T (hg19) ; chr6:g.157201273A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201273A>T , CM000668.2:g.157201273A>T	GRCh38
NC_000006.11:g.157522407A>T , CM000668.1:g.157522407A>T	GRCh37
NC_000006.10:g.157564099A>T	NCBI36
NG_032093.1:g.428344A>T
NG_032093.2:g.428344A>T
NG_066624.1:g.430248A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4889A>T	ENSP00000055163.8:p.Gln1630Leu
ENST00000414678.8:c.4958A>T	ENSP00000412835.3:p.Gln1653Leu
ENST00000637015.2:c.5177A>T	ENSP00000489729.2:p.Gln1726Leu
ENST00000346085.10:c.4928A>T	ENSP00000344546.5:p.Gln1643Leu
ENST00000350026.10:c.4640A>T	ENSP00000055163.7:p.Gln1547Leu
ENST00000414678.7:c.3206A>T	ENSP00000412835.2:p.Gln1069Leu
ENST00000635849.1:c.2369A>T	ENSP00000490948.1:p.Gln790Leu
ENST00000635957.1:c.2000A>T	ENSP00000490385.1:p.Gln667Leu
ENST00000636227.1:n.3511A>T
ENST00000636254.1:n.968A>T
ENST00000636930.2:c.5048A>T MANE Select	ENSP00000490491.2:p.Gln1683Leu
ENST00000636940.1:n.3045A>T
ENST00000637015.1:c.2416A>T
ENST00000637568.1:c.2330A>T
ENST00000637741.1:n.1714A>T
ENST00000637810.1:c.2390A>T	ENSP00000489636.1:p.Gln797Leu
ENST00000637904.1:c.2549A>T	ENSP00000490550.1:p.Gln850Leu
ENST00000647938.1:c.4679A>T	ENSP00000498155.1:p.Gln1560Leu
ENST00000346085.9:c.4679A>T	ENSP00000344546.4:p.Gln1560Leu
ENST00000350026.9:c.4640A>T	ENSP00000055163.7:p.Gln1547Leu
ENST00000414678.6:c.3206A>T	ENSP00000412835.2:p.Gln1069Leu
NM_017519.2:c.4640A>T	NP_059989.2:p.Gln1547Leu
NM_020732.3:c.4679A>T	NP_065783.3:p.Gln1560Leu
XM_005267069.3:c.4799A>T	XP_005267126.2:p.Gln1600Leu
XM_011535984.1:c.3878A>T	XP_011534286.1:p.Gln1293Leu
XM_011535985.1:c.3698A>T	XP_011534287.1:p.Gln1233Leu
XM_011535986.1:c.3458A>T	XP_011534288.1:p.Gln1153Leu
XM_011535987.1:c.3077A>T	XP_011534289.1:p.Gln1026Leu
XM_011535988.1:c.1940A>T	XP_011534290.1:p.Gln647Leu
NM_001346813.1:c.4799A>T	NP_001333742.1:p.Gln1600Leu
NM_001363725.1:c.2549A>T	NP_001350654.1:p.Gln850Leu
XM_011535984.2:c.5009A>T	XP_011534286.2:p.Gln1670Leu
XM_011535988.3:c.1940A>T	XP_011534290.1:p.Gln647Leu
XM_017011103.2:c.4910A>T	XP_016866592.1:p.Gln1637Leu
XM_017011104.1:c.4880A>T	XP_016866593.1:p.Gln1627Leu
XM_017011105.2:c.4850A>T	XP_016866594.1:p.Gln1617Leu
XM_017011106.2:c.4721A>T	XP_016866595.1:p.Gln1574Leu
XM_017011107.2:c.4700A>T	XP_016866596.1:p.Gln1567Leu
XR_002956289.1:n.4995A>T
NM_001363725.2:c.2549A>T	NP_001350654.1:p.Gln850Leu
NM_001371656.1:c.4928A>T	NP_001358585.1:p.Gln1643Leu
NM_001374820.1:c.4928A>T	NP_001361749.1:p.Gln1643Leu
NM_001374828.1:c.5048A>T MANE Select	NP_001361757.1:p.Gln1683Leu
NM_017519.3:c.4889A>T	NP_059989.3:p.Gln1630Leu