Canonical Allele Identifier: CA366242707

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522488T>A (hg19) ; chr6:g.157201354T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201354T>A , CM000668.2:g.157201354T>A	GRCh38
NC_000006.11:g.157522488T>A , CM000668.1:g.157522488T>A	GRCh37
NC_000006.10:g.157564180T>A	NCBI36
NG_032093.1:g.428425T>A
NG_032093.2:g.428425T>A
NG_066624.1:g.430329T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4970T>A	ENSP00000055163.8:p.Val1657Asp
ENST00000414678.8:c.5039T>A	ENSP00000412835.3:p.Val1680Asp
ENST00000637015.2:c.5258T>A	ENSP00000489729.2:p.Val1753Asp
ENST00000346085.10:c.5009T>A	ENSP00000344546.5:p.Val1670Asp
ENST00000350026.10:c.4721T>A	ENSP00000055163.7:p.Val1574Asp
ENST00000414678.7:c.3287T>A	ENSP00000412835.2:p.Val1096Asp
ENST00000635849.1:c.2450T>A	ENSP00000490948.1:p.Val817Asp
ENST00000635957.1:c.2081T>A	ENSP00000490385.1:p.Val694Asp
ENST00000636227.1:n.3592T>A
ENST00000636254.1:n.1049T>A
ENST00000636930.2:c.5129T>A MANE Select	ENSP00000490491.2:p.Val1710Asp
ENST00000636940.1:n.3126T>A
ENST00000637015.1:c.2497T>A
ENST00000637568.1:c.2411T>A
ENST00000637741.1:n.1795T>A
ENST00000637810.1:c.2471T>A	ENSP00000489636.1:p.Val824Asp
ENST00000637904.1:c.2630T>A	ENSP00000490550.1:p.Val877Asp
ENST00000647938.1:c.4760T>A	ENSP00000498155.1:p.Val1587Asp
ENST00000346085.9:c.4760T>A	ENSP00000344546.4:p.Val1587Asp
ENST00000350026.9:c.4721T>A	ENSP00000055163.7:p.Val1574Asp
ENST00000414678.6:c.3287T>A	ENSP00000412835.2:p.Val1096Asp
NM_017519.2:c.4721T>A	NP_059989.2:p.Val1574Asp
NM_020732.3:c.4760T>A	NP_065783.3:p.Val1587Asp
XM_005267069.3:c.4880T>A	XP_005267126.2:p.Val1627Asp
XM_011535984.1:c.3959T>A	XP_011534286.1:p.Val1320Asp
XM_011535985.1:c.3779T>A	XP_011534287.1:p.Val1260Asp
XM_011535986.1:c.3539T>A	XP_011534288.1:p.Val1180Asp
XM_011535987.1:c.3158T>A	XP_011534289.1:p.Val1053Asp
XM_011535988.1:c.2021T>A	XP_011534290.1:p.Val674Asp
NM_001346813.1:c.4880T>A	NP_001333742.1:p.Val1627Asp
NM_001363725.1:c.2630T>A	NP_001350654.1:p.Val877Asp
XM_011535984.2:c.5090T>A	XP_011534286.2:p.Val1697Asp
XM_011535988.3:c.2021T>A	XP_011534290.1:p.Val674Asp
XM_017011103.2:c.4991T>A	XP_016866592.1:p.Val1664Asp
XM_017011104.1:c.4961T>A	XP_016866593.1:p.Val1654Asp
XM_017011105.2:c.4931T>A	XP_016866594.1:p.Val1644Asp
XM_017011106.2:c.4802T>A	XP_016866595.1:p.Val1601Asp
XM_017011107.2:c.4781T>A	XP_016866596.1:p.Val1594Asp
XR_002956289.1:n.5076T>A
NM_001363725.2:c.2630T>A	NP_001350654.1:p.Val877Asp
NM_001371656.1:c.5009T>A	NP_001358585.1:p.Val1670Asp
NM_001374820.1:c.5009T>A	NP_001361749.1:p.Val1670Asp
NM_001374828.1:c.5129T>A MANE Select	NP_001361757.1:p.Val1710Asp
NM_017519.3:c.4970T>A	NP_059989.3:p.Val1657Asp