Canonical Allele Identifier: CA366388903

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469896G>T (hg19) ; chr6:g.157148762G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148762G>T , CM000668.2:g.157148762G>T	GRCh38
NC_000006.11:g.157469896G>T , CM000668.1:g.157469896G>T	GRCh37
NC_000006.10:g.157511588G>T	NCBI36
NG_032093.1:g.375833G>T
NG_032093.2:g.375833G>T
NG_066624.1:g.377737G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2900G>T	ENSP00000055163.8:p.Gly967Val
ENST00000414678.8:c.2810G>T	ENSP00000412835.3:p.Gly937Val
ENST00000637015.2:c.2900G>T	ENSP00000489729.2:p.Gly967Val
ENST00000319584.11:c.914G>T	ENSP00000313006.7:p.Gly305Val
ENST00000346085.10:c.2939G>T	ENSP00000344546.5:p.Gly980Val
ENST00000350026.10:c.2651G>T	ENSP00000055163.7:p.Gly884Val
ENST00000414678.7:c.1058G>T	ENSP00000412835.2:p.Gly353Val
ENST00000452544.2:n.801G>T
ENST00000635849.1:c.221G>T	ENSP00000490948.1:p.Gly74Val
ENST00000636426.1:n.34G>T
ENST00000636930.2:c.2900G>T MANE Select	ENSP00000490491.2:p.Gly967Val
ENST00000637015.1:c.139G>T
ENST00000637810.1:c.401G>T	ENSP00000489636.1:p.Gly134Val
ENST00000637904.1:c.401G>T	ENSP00000490550.1:p.Gly134Val
ENST00000647938.1:c.2690G>T	ENSP00000498155.1:p.Gly897Val
ENST00000674190.1:n.1649G>T
ENST00000319584.10:c.917G>T	ENSP00000313006.6:p.Gly306Val
ENST00000346085.9:c.2690G>T	ENSP00000344546.4:p.Gly897Val
ENST00000350026.9:c.2651G>T	ENSP00000055163.7:p.Gly884Val
ENST00000414678.6:c.1058G>T	ENSP00000412835.2:p.Gly353Val
ENST00000452544.1:n.747G>T
NM_017519.2:c.2651G>T	NP_059989.2:p.Gly884Val
NM_020732.3:c.2690G>T	NP_065783.3:p.Gly897Val
XM_005267069.3:c.2651G>T	XP_005267126.2:p.Gly884Val
XM_011535984.1:c.1601G>T	XP_011534286.1:p.Gly534Val
XM_011535985.1:c.1421G>T	XP_011534287.1:p.Gly474Val
XM_011535986.1:c.1181G>T	XP_011534288.1:p.Gly394Val
XM_011535987.1:c.800G>T	XP_011534289.1:p.Gly267Val
XM_011535988.1:c.-20+15555G>T	XP_011534290.1:n.-20+15555G>T
NM_001346813.1:c.2651G>T	NP_001333742.1:p.Gly884Val
NM_001363725.1:c.401G>T	NP_001350654.1:p.Gly134Val
XM_011535984.2:c.2732G>T	XP_011534286.2:p.Gly911Val
XM_011535988.3:c.-20+15555G>T	XP_011534290.1:n.-20+15555G>T
XM_017011103.2:c.2732G>T	XP_016866592.1:p.Gly911Val
XM_017011104.1:c.2732G>T	XP_016866593.1:p.Gly911Val
XM_017011105.2:c.2732G>T	XP_016866594.1:p.Gly911Val
XM_017011106.2:c.2732G>T	XP_016866595.1:p.Gly911Val
XM_017011107.2:c.2552G>T	XP_016866596.1:p.Gly851Val
XR_002956289.1:n.2815G>T
NM_001363725.2:c.401G>T	NP_001350654.1:p.Gly134Val
NM_001371656.1:c.2939G>T	NP_001358585.1:p.Gly980Val
NM_001374820.1:c.2939G>T	NP_001361749.1:p.Gly980Val
NM_001374828.1:c.2900G>T MANE Select	NP_001361757.1:p.Gly967Val
NM_017519.3:c.2900G>T	NP_059989.3:p.Gly967Val