Canonical Allele Identifier: CA366387084

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084701G>T , CM000668.2:g.157084701G>T	GRCh38
NC_000006.11:g.157405835G>T , CM000668.1:g.157405835G>T	GRCh37
NC_000006.10:g.157447527G>T	NCBI36
NG_032093.1:g.311772G>T
NG_032093.2:g.311772G>T
NG_066624.1:g.313676G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.2287G>T MANE Select	NP_001361757.1:p.Glu763Ter
ENST00000636930.2:c.2287G>T MANE Select	ENSP00000490491.2:p.Glu763Ter
NM_001346813.1:c.2038G>T	NP_001333742.1:p.Glu680Ter
NM_001363725.1:c.-213G>T	NP_001350654.1:n.-213G>T
NM_001363725.2:c.-213G>T	NP_001350654.1:n.-213G>T
NM_001371656.1:c.2326G>T	NP_001358585.1:p.Glu776Ter
NM_001374820.1:c.2326G>T	NP_001361749.1:p.Glu776Ter
NM_017519.2:c.2038G>T	NP_059989.2:p.Glu680Ter
NM_017519.3:c.2287G>T	NP_059989.3:p.Glu763Ter
NM_020732.3:c.2077G>T	NP_065783.3:p.Glu693Ter
ENST00000319584.10:c.304G>T	ENSP00000313006.6:p.Glu102Ter
ENST00000319584.11:c.301G>T	ENSP00000313006.7:p.Glu101Ter
ENST00000346085.10:c.2326G>T	ENSP00000344546.5:p.Glu776Ter
ENST00000346085.9:c.2077G>T	ENSP00000344546.4:p.Glu693Ter
ENST00000350026.10:c.2038G>T	ENSP00000055163.7:p.Glu680Ter
ENST00000350026.11:c.2287G>T	ENSP00000055163.8:p.Glu763Ter
ENST00000350026.9:c.2038G>T	ENSP00000055163.7:p.Glu680Ter
ENST00000414678.6:c.535G>T	ENSP00000412835.2:p.Glu179Ter
ENST00000414678.7:c.535G>T	ENSP00000412835.2:p.Glu179Ter
ENST00000414678.8:c.2287G>T	ENSP00000412835.3:p.Glu763Ter
ENST00000452544.1:n.146G>T
ENST00000452544.2:n.188G>T
ENST00000635849.1:c.-213G>T	ENSP00000490948.1:n.-213G>T
ENST00000637003.1:c.-213G>T	ENSP00000489666.1:n.-213G>T
ENST00000637015.2:c.2287G>T	ENSP00000489729.2:p.Glu763Ter
ENST00000637904.1:c.-213G>T	ENSP00000490550.1:n.-213G>T
ENST00000647938.1:c.2077G>T	ENSP00000498155.1:p.Glu693Ter
ENST00000674190.1:n.1036G>T
XM_005267069.3:c.2038G>T	XP_005267126.2:p.Glu680Ter
XM_011535984.1:c.988G>T	XP_011534286.1:p.Glu330Ter
XM_011535984.2:c.2119G>T	XP_011534286.2:p.Glu707Ter
XM_011535985.1:c.988G>T	XP_011534287.1:p.Glu330Ter
XM_011535986.1:c.568G>T	XP_011534288.1:p.Glu190Ter
XM_011535987.1:c.187G>T	XP_011534289.1:p.Glu63Ter
XM_017011103.2:c.2119G>T	XP_016866592.1:p.Glu707Ter
XM_017011104.1:c.2119G>T	XP_016866593.1:p.Glu707Ter
XM_017011105.2:c.2119G>T	XP_016866594.1:p.Glu707Ter
XM_017011106.2:c.2119G>T	XP_016866595.1:p.Glu707Ter
XM_017011107.2:c.2119G>T	XP_016866596.1:p.Glu707Ter
XR_002956289.1:n.2202G>T