Canonical Allele Identifier: CA452780815

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502267G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181133G>T , CM000668.2:g.157181133G>T	GRCh38
NC_000006.11:g.157502267G>T , CM000668.1:g.157502267G>T	GRCh37
NC_000006.10:g.157543959G>T	NCBI36
NG_032093.1:g.408204G>T
NG_032093.2:g.408204G>T
NG_066624.1:g.410108G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3510G>T	ENSP00000055163.8:p.Leu1170=
ENST00000414678.8:c.3579G>T	ENSP00000412835.3:p.Leu1193=
ENST00000637015.2:c.3798G>T	ENSP00000489729.2:p.Leu1266=
ENST00000319584.11:c.1683G>T	ENSP00000313006.7:p.Leu561=
ENST00000346085.10:c.3549G>T	ENSP00000344546.5:p.Leu1183=
ENST00000350026.10:c.3261G>T	ENSP00000055163.7:p.Leu1087=
ENST00000414678.7:c.1827G>T	ENSP00000412835.2:p.Leu609=
ENST00000635849.1:c.990G>T	ENSP00000490948.1:p.Leu330=
ENST00000635957.1:c.624G>T	ENSP00000490385.1:p.Leu208=
ENST00000636930.2:c.3669G>T MANE Select	ENSP00000490491.2:p.Leu1223=
ENST00000636940.1:n.1666G>T
ENST00000637015.1:c.1037G>T
ENST00000637568.1:c.951G>T
ENST00000637741.1:n.335G>T
ENST00000637810.1:c.1011G>T	ENSP00000489636.1:p.Leu337=
ENST00000637904.1:c.1170G>T	ENSP00000490550.1:p.Leu390=
ENST00000647938.1:c.3300G>T	ENSP00000498155.1:p.Leu1100=
ENST00000319584.10:c.1686G>T	ENSP00000313006.6:p.Leu562=
ENST00000346085.9:c.3300G>T	ENSP00000344546.4:p.Leu1100=
ENST00000350026.9:c.3261G>T	ENSP00000055163.7:p.Leu1087=
ENST00000400790.3:c.462G>T	ENSP00000383596.3:p.Leu154=
ENST00000414678.6:c.1827G>T	ENSP00000412835.2:p.Leu609=
ENST00000478761.3:c.871G>T
NM_017519.2:c.3261G>T	NP_059989.2:p.Leu1087=
NM_020732.3:c.3300G>T	NP_065783.3:p.Leu1100=
XM_005267069.3:c.3420G>T	XP_005267126.2:p.Leu1140=
XM_011535984.1:c.2499G>T	XP_011534286.1:p.Leu833=
XM_011535985.1:c.2319G>T	XP_011534287.1:p.Leu773=
XM_011535986.1:c.2079G>T	XP_011534288.1:p.Leu693=
XM_011535987.1:c.1698G>T	XP_011534289.1:p.Leu566=
XM_011535988.1:c.561G>T	XP_011534290.1:p.Leu187=
NM_001346813.1:c.3420G>T	NP_001333742.1:p.Leu1140=
NM_001363725.1:c.1170G>T	NP_001350654.1:p.Leu390=
XM_011535984.2:c.3630G>T	XP_011534286.2:p.Leu1210=
XM_011535988.3:c.561G>T	XP_011534290.1:p.Leu187=
XM_017011103.2:c.3531G>T	XP_016866592.1:p.Leu1177=
XM_017011104.1:c.3501G>T	XP_016866593.1:p.Leu1167=
XM_017011105.2:c.3471G>T	XP_016866594.1:p.Leu1157=
XM_017011106.2:c.3342G>T	XP_016866595.1:p.Leu1114=
XM_017011107.2:c.3321G>T	XP_016866596.1:p.Leu1107=
XR_002956289.1:n.3713G>T
NM_001363725.2:c.1170G>T	NP_001350654.1:p.Leu390=
NM_001371656.1:c.3549G>T	NP_001358585.1:p.Leu1183=
NM_001374820.1:c.3549G>T	NP_001361749.1:p.Leu1183=
NM_001374828.1:c.3669G>T MANE Select	NP_001361757.1:p.Leu1223=
NM_017519.3:c.3510G>T	NP_059989.3:p.Leu1170=