Canonical Allele Identifier: CA366242710

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4970T>C	ENSP00000055163.8:p.Val1657Ala
ENST00000414678.8:c.5039T>C	ENSP00000412835.3:p.Val1680Ala
ENST00000637015.2:c.5258T>C	ENSP00000489729.2:p.Val1753Ala
ENST00000346085.10:c.5009T>C	ENSP00000344546.5:p.Val1670Ala
ENST00000350026.10:c.4721T>C	ENSP00000055163.7:p.Val1574Ala
ENST00000414678.7:c.3287T>C	ENSP00000412835.2:p.Val1096Ala
ENST00000635849.1:c.2450T>C	ENSP00000490948.1:p.Val817Ala
ENST00000635957.1:c.2081T>C	ENSP00000490385.1:p.Val694Ala
ENST00000636227.1:n.3592T>C
ENST00000636254.1:n.1049T>C
ENST00000636930.2:c.5129T>C MANE Select	ENSP00000490491.2:p.Val1710Ala
ENST00000636940.1:n.3126T>C
ENST00000637015.1:c.2497T>C
ENST00000637568.1:c.2411T>C
ENST00000637741.1:n.1795T>C
ENST00000637810.1:c.2471T>C	ENSP00000489636.1:p.Val824Ala
ENST00000637904.1:c.2630T>C	ENSP00000490550.1:p.Val877Ala
ENST00000647938.1:c.4760T>C	ENSP00000498155.1:p.Val1587Ala
ENST00000346085.9:c.4760T>C	ENSP00000344546.4:p.Val1587Ala
ENST00000350026.9:c.4721T>C	ENSP00000055163.7:p.Val1574Ala
ENST00000414678.6:c.3287T>C	ENSP00000412835.2:p.Val1096Ala
NM_017519.2:c.4721T>C	NP_059989.2:p.Val1574Ala
NM_020732.3:c.4760T>C	NP_065783.3:p.Val1587Ala
XM_005267069.3:c.4880T>C	XP_005267126.2:p.Val1627Ala
XM_011535984.1:c.3959T>C	XP_011534286.1:p.Val1320Ala
XM_011535985.1:c.3779T>C	XP_011534287.1:p.Val1260Ala
XM_011535986.1:c.3539T>C	XP_011534288.1:p.Val1180Ala
XM_011535987.1:c.3158T>C	XP_011534289.1:p.Val1053Ala
XM_011535988.1:c.2021T>C	XP_011534290.1:p.Val674Ala
NM_001346813.1:c.4880T>C	NP_001333742.1:p.Val1627Ala
NM_001363725.1:c.2630T>C	NP_001350654.1:p.Val877Ala
XM_011535984.2:c.5090T>C	XP_011534286.2:p.Val1697Ala
XM_011535988.3:c.2021T>C	XP_011534290.1:p.Val674Ala
XM_017011103.2:c.4991T>C	XP_016866592.1:p.Val1664Ala
XM_017011104.1:c.4961T>C	XP_016866593.1:p.Val1654Ala
XM_017011105.2:c.4931T>C	XP_016866594.1:p.Val1644Ala
XM_017011106.2:c.4802T>C	XP_016866595.1:p.Val1601Ala
XM_017011107.2:c.4781T>C	XP_016866596.1:p.Val1594Ala
XR_002956289.1:n.5076T>C
NM_001363725.2:c.2630T>C	NP_001350654.1:p.Val877Ala
NM_001371656.1:c.5009T>C	NP_001358585.1:p.Val1670Ala
NM_001374820.1:c.5009T>C	NP_001361749.1:p.Val1670Ala
NM_001374828.1:c.5129T>C MANE Select	NP_001361757.1:p.Val1710Ala
NM_017519.3:c.4970T>C	NP_059989.3:p.Val1657Ala