Canonical Allele Identifier: CA452990074

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469858A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148724A>T , CM000668.2:g.157148724A>T	GRCh38
NC_000006.11:g.157469858A>T , CM000668.1:g.157469858A>T	GRCh37
NC_000006.10:g.157511550A>T	NCBI36
NG_032093.1:g.375795A>T
NG_032093.2:g.375795A>T
NG_066624.1:g.377699A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2862A>T	ENSP00000055163.8:p.Gly954=
ENST00000414678.8:c.2772A>T	ENSP00000412835.3:p.Gly924=
ENST00000637015.2:c.2862A>T	ENSP00000489729.2:p.Gly954=
ENST00000319584.11:c.876A>T	ENSP00000313006.7:p.Gly292=
ENST00000346085.10:c.2901A>T	ENSP00000344546.5:p.Gly967=
ENST00000350026.10:c.2613A>T	ENSP00000055163.7:p.Gly871=
ENST00000414678.7:c.1020A>T	ENSP00000412835.2:p.Gly340=
ENST00000452544.2:n.763A>T
ENST00000635849.1:c.183A>T	ENSP00000490948.1:p.Gly61=
ENST00000636930.2:c.2862A>T MANE Select	ENSP00000490491.2:p.Gly954=
ENST00000637015.1:c.101A>T
ENST00000637810.1:c.363A>T	ENSP00000489636.1:p.Gly121=
ENST00000637904.1:c.363A>T	ENSP00000490550.1:p.Gly121=
ENST00000647938.1:c.2652A>T	ENSP00000498155.1:p.Gly884=
ENST00000674190.1:n.1611A>T
ENST00000319584.10:c.879A>T	ENSP00000313006.6:p.Gly293=
ENST00000346085.9:c.2652A>T	ENSP00000344546.4:p.Gly884=
ENST00000350026.9:c.2613A>T	ENSP00000055163.7:p.Gly871=
ENST00000414678.6:c.1020A>T	ENSP00000412835.2:p.Gly340=
ENST00000452544.1:n.709A>T
NM_017519.2:c.2613A>T	NP_059989.2:p.Gly871=
NM_020732.3:c.2652A>T	NP_065783.3:p.Gly884=
XM_005267069.3:c.2613A>T	XP_005267126.2:p.Gly871=
XM_011535984.1:c.1563A>T	XP_011534286.1:p.Gly521=
XM_011535985.1:c.1383A>T	XP_011534287.1:p.Gly461=
XM_011535986.1:c.1143A>T	XP_011534288.1:p.Gly381=
XM_011535987.1:c.762A>T	XP_011534289.1:p.Gly254=
XM_011535988.1:c.-20+15517A>T	XP_011534290.1:n.-20+15517A>T
NM_001346813.1:c.2613A>T	NP_001333742.1:p.Gly871=
NM_001363725.1:c.363A>T	NP_001350654.1:p.Gly121=
XM_011535984.2:c.2694A>T	XP_011534286.2:p.Gly898=
XM_011535988.3:c.-20+15517A>T	XP_011534290.1:n.-20+15517A>T
XM_017011103.2:c.2694A>T	XP_016866592.1:p.Gly898=
XM_017011104.1:c.2694A>T	XP_016866593.1:p.Gly898=
XM_017011105.2:c.2694A>T	XP_016866594.1:p.Gly898=
XM_017011106.2:c.2694A>T	XP_016866595.1:p.Gly898=
XM_017011107.2:c.2514A>T	XP_016866596.1:p.Gly838=
XR_002956289.1:n.2777A>T
NM_001363725.2:c.363A>T	NP_001350654.1:p.Gly121=
NM_001371656.1:c.2901A>T	NP_001358585.1:p.Gly967=
NM_001374820.1:c.2901A>T	NP_001361749.1:p.Gly967=
NM_001374828.1:c.2862A>T MANE Select	NP_001361757.1:p.Gly954=
NM_017519.3:c.2862A>T	NP_059989.3:p.Gly954=