Canonical Allele Identifier: CA452780827

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502288C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181154C>G , CM000668.2:g.157181154C>G	GRCh38
NC_000006.11:g.157502288C>G , CM000668.1:g.157502288C>G	GRCh37
NC_000006.10:g.157543980C>G	NCBI36
NG_032093.1:g.408225C>G
NG_032093.2:g.408225C>G
NG_066624.1:g.410129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3531C>G	ENSP00000055163.8:p.Val1177=
ENST00000414678.8:c.3600C>G	ENSP00000412835.3:p.Val1200=
ENST00000637015.2:c.3819C>G	ENSP00000489729.2:p.Val1273=
ENST00000319584.11:c.1704C>G	ENSP00000313006.7:p.Val568=
ENST00000346085.10:c.3570C>G	ENSP00000344546.5:p.Val1190=
ENST00000350026.10:c.3282C>G	ENSP00000055163.7:p.Val1094=
ENST00000414678.7:c.1848C>G	ENSP00000412835.2:p.Val616=
ENST00000635849.1:c.1011C>G	ENSP00000490948.1:p.Val337=
ENST00000635957.1:c.645C>G	ENSP00000490385.1:p.Val215=
ENST00000636930.2:c.3690C>G MANE Select	ENSP00000490491.2:p.Val1230=
ENST00000636940.1:n.1687C>G
ENST00000637015.1:c.1058C>G
ENST00000637568.1:c.972C>G
ENST00000637741.1:n.356C>G
ENST00000637810.1:c.1032C>G	ENSP00000489636.1:p.Val344=
ENST00000637904.1:c.1191C>G	ENSP00000490550.1:p.Val397=
ENST00000647938.1:c.3321C>G	ENSP00000498155.1:p.Val1107=
ENST00000319584.10:c.1707C>G	ENSP00000313006.6:p.Val569=
ENST00000346085.9:c.3321C>G	ENSP00000344546.4:p.Val1107=
ENST00000350026.9:c.3282C>G	ENSP00000055163.7:p.Val1094=
ENST00000400790.3:c.483C>G	ENSP00000383596.3:p.Val161=
ENST00000414678.6:c.1848C>G	ENSP00000412835.2:p.Val616=
ENST00000478761.3:c.892C>G
NM_017519.2:c.3282C>G	NP_059989.2:p.Val1094=
NM_020732.3:c.3321C>G	NP_065783.3:p.Val1107=
XM_005267069.3:c.3441C>G	XP_005267126.2:p.Val1147=
XM_011535984.1:c.2520C>G	XP_011534286.1:p.Val840=
XM_011535985.1:c.2340C>G	XP_011534287.1:p.Val780=
XM_011535986.1:c.2100C>G	XP_011534288.1:p.Val700=
XM_011535987.1:c.1719C>G	XP_011534289.1:p.Val573=
XM_011535988.1:c.582C>G	XP_011534290.1:p.Val194=
NM_001346813.1:c.3441C>G	NP_001333742.1:p.Val1147=
NM_001363725.1:c.1191C>G	NP_001350654.1:p.Val397=
XM_011535984.2:c.3651C>G	XP_011534286.2:p.Val1217=
XM_011535988.3:c.582C>G	XP_011534290.1:p.Val194=
XM_017011103.2:c.3552C>G	XP_016866592.1:p.Val1184=
XM_017011104.1:c.3522C>G	XP_016866593.1:p.Val1174=
XM_017011105.2:c.3492C>G	XP_016866594.1:p.Val1164=
XM_017011106.2:c.3363C>G	XP_016866595.1:p.Val1121=
XM_017011107.2:c.3342C>G	XP_016866596.1:p.Val1114=
XR_002956289.1:n.3734C>G
NM_001363725.2:c.1191C>G	NP_001350654.1:p.Val397=
NM_001371656.1:c.3570C>G	NP_001358585.1:p.Val1190=
NM_001374820.1:c.3570C>G	NP_001361749.1:p.Val1190=
NM_001374828.1:c.3690C>G MANE Select	NP_001361757.1:p.Val1230=
NM_017519.3:c.3531C>G	NP_059989.3:p.Val1177=