Canonical Allele Identifier: CA366240884

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521903A>C (hg19) ; chr6:g.157200769A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200769A>C , CM000668.2:g.157200769A>C	GRCh38
NC_000006.11:g.157521903A>C , CM000668.1:g.157521903A>C	GRCh37
NC_000006.10:g.157563595A>C	NCBI36
NG_032093.1:g.427840A>C
NG_032093.2:g.427840A>C
NG_066624.1:g.429744A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4385A>C	ENSP00000055163.8:p.Tyr1462Ser
ENST00000414678.8:c.4454A>C	ENSP00000412835.3:p.Tyr1485Ser
ENST00000637015.2:c.4673A>C	ENSP00000489729.2:p.Tyr1558Ser
ENST00000346085.10:c.4424A>C	ENSP00000344546.5:p.Tyr1475Ser
ENST00000350026.10:c.4136A>C	ENSP00000055163.7:p.Tyr1379Ser
ENST00000414678.7:c.2702A>C	ENSP00000412835.2:p.Tyr901Ser
ENST00000635849.1:c.1865A>C	ENSP00000490948.1:p.Tyr622Ser
ENST00000635957.1:c.1496A>C	ENSP00000490385.1:p.Tyr499Ser
ENST00000636227.1:n.3007A>C
ENST00000636254.1:n.464A>C
ENST00000636930.2:c.4544A>C MANE Select	ENSP00000490491.2:p.Tyr1515Ser
ENST00000636940.1:n.2541A>C
ENST00000637015.1:c.1912A>C
ENST00000637568.1:c.1826A>C
ENST00000637741.1:n.1210A>C
ENST00000637810.1:c.1886A>C	ENSP00000489636.1:p.Tyr629Ser
ENST00000637904.1:c.2045A>C	ENSP00000490550.1:p.Tyr682Ser
ENST00000647938.1:c.4175A>C	ENSP00000498155.1:p.Tyr1392Ser
ENST00000346085.9:c.4175A>C	ENSP00000344546.4:p.Tyr1392Ser
ENST00000350026.9:c.4136A>C	ENSP00000055163.7:p.Tyr1379Ser
ENST00000414678.6:c.2702A>C	ENSP00000412835.2:p.Tyr901Ser
NM_017519.2:c.4136A>C	NP_059989.2:p.Tyr1379Ser
NM_020732.3:c.4175A>C	NP_065783.3:p.Tyr1392Ser
XM_005267069.3:c.4295A>C	XP_005267126.2:p.Tyr1432Ser
XM_011535984.1:c.3374A>C	XP_011534286.1:p.Tyr1125Ser
XM_011535985.1:c.3194A>C	XP_011534287.1:p.Tyr1065Ser
XM_011535986.1:c.2954A>C	XP_011534288.1:p.Tyr985Ser
XM_011535987.1:c.2573A>C	XP_011534289.1:p.Tyr858Ser
XM_011535988.1:c.1436A>C	XP_011534290.1:p.Tyr479Ser
NM_001346813.1:c.4295A>C	NP_001333742.1:p.Tyr1432Ser
NM_001363725.1:c.2045A>C	NP_001350654.1:p.Tyr682Ser
XM_011535984.2:c.4505A>C	XP_011534286.2:p.Tyr1502Ser
XM_011535988.3:c.1436A>C	XP_011534290.1:p.Tyr479Ser
XM_017011103.2:c.4406A>C	XP_016866592.1:p.Tyr1469Ser
XM_017011104.1:c.4376A>C	XP_016866593.1:p.Tyr1459Ser
XM_017011105.2:c.4346A>C	XP_016866594.1:p.Tyr1449Ser
XM_017011106.2:c.4217A>C	XP_016866595.1:p.Tyr1406Ser
XM_017011107.2:c.4196A>C	XP_016866596.1:p.Tyr1399Ser
XR_002956289.1:n.4491A>C
NM_001363725.2:c.2045A>C	NP_001350654.1:p.Tyr682Ser
NM_001371656.1:c.4424A>C	NP_001358585.1:p.Tyr1475Ser
NM_001374820.1:c.4424A>C	NP_001361749.1:p.Tyr1475Ser
NM_001374828.1:c.4544A>C MANE Select	NP_001361757.1:p.Tyr1515Ser
NM_017519.3:c.4385A>C	NP_059989.3:p.Tyr1462Ser