Canonical Allele Identifier: CA366235327

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511261A>C (hg19) ; chr6:g.157190127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190127A>C , CM000668.2:g.157190127A>C	GRCh38
NC_000006.11:g.157511261A>C , CM000668.1:g.157511261A>C	GRCh37
NC_000006.10:g.157552953A>C	NCBI36
NG_032093.1:g.417198A>C
NG_032093.2:g.417198A>C
NG_066624.1:g.419102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3989A>C	ENSP00000055163.8:p.Tyr1330Ser
ENST00000414678.8:c.4058A>C	ENSP00000412835.3:p.Tyr1353Ser
ENST00000637015.2:c.4277A>C	ENSP00000489729.2:p.Tyr1426Ser
ENST00000346085.10:c.4028A>C	ENSP00000344546.5:p.Tyr1343Ser
ENST00000350026.10:c.3740A>C	ENSP00000055163.7:p.Tyr1247Ser
ENST00000414678.7:c.2306A>C	ENSP00000412835.2:p.Tyr769Ser
ENST00000635849.1:c.1469A>C	ENSP00000490948.1:p.Tyr490Ser
ENST00000635957.1:c.1100A>C	ENSP00000490385.1:p.Tyr367Ser
ENST00000636930.2:c.4148A>C MANE Select	ENSP00000490491.2:p.Tyr1383Ser
ENST00000636940.1:n.2145A>C
ENST00000637015.1:c.1516A>C
ENST00000637568.1:c.1430A>C
ENST00000637741.1:n.814A>C
ENST00000637810.1:c.1490A>C	ENSP00000489636.1:p.Tyr497Ser
ENST00000637904.1:c.1649A>C	ENSP00000490550.1:p.Tyr550Ser
ENST00000647938.1:c.3779A>C	ENSP00000498155.1:p.Tyr1260Ser
ENST00000346085.9:c.3779A>C	ENSP00000344546.4:p.Tyr1260Ser
ENST00000350026.9:c.3740A>C	ENSP00000055163.7:p.Tyr1247Ser
ENST00000414678.6:c.2306A>C	ENSP00000412835.2:p.Tyr769Ser
NM_017519.2:c.3740A>C	NP_059989.2:p.Tyr1247Ser
NM_020732.3:c.3779A>C	NP_065783.3:p.Tyr1260Ser
XM_005267069.3:c.3899A>C	XP_005267126.2:p.Tyr1300Ser
XM_011535984.1:c.2978A>C	XP_011534286.1:p.Tyr993Ser
XM_011535985.1:c.2798A>C	XP_011534287.1:p.Tyr933Ser
XM_011535986.1:c.2558A>C	XP_011534288.1:p.Tyr853Ser
XM_011535987.1:c.2177A>C	XP_011534289.1:p.Tyr726Ser
XM_011535988.1:c.1040A>C	XP_011534290.1:p.Tyr347Ser
NM_001346813.1:c.3899A>C	NP_001333742.1:p.Tyr1300Ser
NM_001363725.1:c.1649A>C	NP_001350654.1:p.Tyr550Ser
XM_011535984.2:c.4109A>C	XP_011534286.2:p.Tyr1370Ser
XM_011535988.3:c.1040A>C	XP_011534290.1:p.Tyr347Ser
XM_017011103.2:c.4010A>C	XP_016866592.1:p.Tyr1337Ser
XM_017011104.1:c.3980A>C	XP_016866593.1:p.Tyr1327Ser
XM_017011105.2:c.3950A>C	XP_016866594.1:p.Tyr1317Ser
XM_017011106.2:c.3821A>C	XP_016866595.1:p.Tyr1274Ser
XM_017011107.2:c.3800A>C	XP_016866596.1:p.Tyr1267Ser
XR_002956289.1:n.4192A>C
NM_001363725.2:c.1649A>C	NP_001350654.1:p.Tyr550Ser
NM_001371656.1:c.4028A>C	NP_001358585.1:p.Tyr1343Ser
NM_001374820.1:c.4028A>C	NP_001361749.1:p.Tyr1343Ser
NM_001374828.1:c.4148A>C MANE Select	NP_001361757.1:p.Tyr1383Ser
NM_017519.3:c.3989A>C	NP_059989.3:p.Tyr1330Ser