Canonical Allele Identifier: CA366242712

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4970T>G	ENSP00000055163.8:p.Val1657Gly
ENST00000414678.8:c.5039T>G	ENSP00000412835.3:p.Val1680Gly
ENST00000637015.2:c.5258T>G	ENSP00000489729.2:p.Val1753Gly
ENST00000346085.10:c.5009T>G	ENSP00000344546.5:p.Val1670Gly
ENST00000350026.10:c.4721T>G	ENSP00000055163.7:p.Val1574Gly
ENST00000414678.7:c.3287T>G	ENSP00000412835.2:p.Val1096Gly
ENST00000635849.1:c.2450T>G	ENSP00000490948.1:p.Val817Gly
ENST00000635957.1:c.2081T>G	ENSP00000490385.1:p.Val694Gly
ENST00000636227.1:n.3592T>G
ENST00000636254.1:n.1049T>G
ENST00000636930.2:c.5129T>G MANE Select	ENSP00000490491.2:p.Val1710Gly
ENST00000636940.1:n.3126T>G
ENST00000637015.1:c.2497T>G
ENST00000637568.1:c.2411T>G
ENST00000637741.1:n.1795T>G
ENST00000637810.1:c.2471T>G	ENSP00000489636.1:p.Val824Gly
ENST00000637904.1:c.2630T>G	ENSP00000490550.1:p.Val877Gly
ENST00000647938.1:c.4760T>G	ENSP00000498155.1:p.Val1587Gly
ENST00000346085.9:c.4760T>G	ENSP00000344546.4:p.Val1587Gly
ENST00000350026.9:c.4721T>G	ENSP00000055163.7:p.Val1574Gly
ENST00000414678.6:c.3287T>G	ENSP00000412835.2:p.Val1096Gly
NM_017519.2:c.4721T>G	NP_059989.2:p.Val1574Gly
NM_020732.3:c.4760T>G	NP_065783.3:p.Val1587Gly
XM_005267069.3:c.4880T>G	XP_005267126.2:p.Val1627Gly
XM_011535984.1:c.3959T>G	XP_011534286.1:p.Val1320Gly
XM_011535985.1:c.3779T>G	XP_011534287.1:p.Val1260Gly
XM_011535986.1:c.3539T>G	XP_011534288.1:p.Val1180Gly
XM_011535987.1:c.3158T>G	XP_011534289.1:p.Val1053Gly
XM_011535988.1:c.2021T>G	XP_011534290.1:p.Val674Gly
NM_001346813.1:c.4880T>G	NP_001333742.1:p.Val1627Gly
NM_001363725.1:c.2630T>G	NP_001350654.1:p.Val877Gly
XM_011535984.2:c.5090T>G	XP_011534286.2:p.Val1697Gly
XM_011535988.3:c.2021T>G	XP_011534290.1:p.Val674Gly
XM_017011103.2:c.4991T>G	XP_016866592.1:p.Val1664Gly
XM_017011104.1:c.4961T>G	XP_016866593.1:p.Val1654Gly
XM_017011105.2:c.4931T>G	XP_016866594.1:p.Val1644Gly
XM_017011106.2:c.4802T>G	XP_016866595.1:p.Val1601Gly
XM_017011107.2:c.4781T>G	XP_016866596.1:p.Val1594Gly
XR_002956289.1:n.5076T>G
NM_001363725.2:c.2630T>G	NP_001350654.1:p.Val877Gly
NM_001371656.1:c.5009T>G	NP_001358585.1:p.Val1670Gly
NM_001374820.1:c.5009T>G	NP_001361749.1:p.Val1670Gly
NM_001374828.1:c.5129T>G MANE Select	NP_001361757.1:p.Val1710Gly
NM_017519.3:c.4970T>G	NP_059989.3:p.Val1657Gly