Canonical Allele Identifier: CA366242947

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522537A>C (hg19) ; chr6:g.157201403A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201403A>C , CM000668.2:g.157201403A>C	GRCh38
NC_000006.11:g.157522537A>C , CM000668.1:g.157522537A>C	GRCh37
NC_000006.10:g.157564229A>C	NCBI36
NG_032093.1:g.428474A>C
NG_032093.2:g.428474A>C
NG_066624.1:g.430378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5019A>C	ENSP00000055163.8:p.Arg1673Ser
ENST00000414678.8:c.5088A>C	ENSP00000412835.3:p.Arg1696Ser
ENST00000637015.2:c.5307A>C	ENSP00000489729.2:p.Arg1769Ser
ENST00000346085.10:c.5058A>C	ENSP00000344546.5:p.Arg1686Ser
ENST00000350026.10:c.4770A>C	ENSP00000055163.7:p.Arg1590Ser
ENST00000414678.7:c.3336A>C	ENSP00000412835.2:p.Arg1112Ser
ENST00000635849.1:c.2499A>C	ENSP00000490948.1:p.Arg833Ser
ENST00000635957.1:c.2130A>C	ENSP00000490385.1:p.Arg710Ser
ENST00000636227.1:n.3641A>C
ENST00000636254.1:n.1098A>C
ENST00000636930.2:c.5178A>C MANE Select	ENSP00000490491.2:p.Arg1726Ser
ENST00000636940.1:n.3175A>C
ENST00000637015.1:c.2546A>C
ENST00000637568.1:c.2460A>C
ENST00000637741.1:n.1844A>C
ENST00000637810.1:c.2520A>C	ENSP00000489636.1:p.Arg840Ser
ENST00000637904.1:c.2679A>C	ENSP00000490550.1:p.Arg893Ser
ENST00000647938.1:c.4809A>C	ENSP00000498155.1:p.Arg1603Ser
ENST00000346085.9:c.4809A>C	ENSP00000344546.4:p.Arg1603Ser
ENST00000350026.9:c.4770A>C	ENSP00000055163.7:p.Arg1590Ser
ENST00000414678.6:c.3336A>C	ENSP00000412835.2:p.Arg1112Ser
NM_017519.2:c.4770A>C	NP_059989.2:p.Arg1590Ser
NM_020732.3:c.4809A>C	NP_065783.3:p.Arg1603Ser
XM_005267069.3:c.4929A>C	XP_005267126.2:p.Arg1643Ser
XM_011535984.1:c.4008A>C	XP_011534286.1:p.Arg1336Ser
XM_011535985.1:c.3828A>C	XP_011534287.1:p.Arg1276Ser
XM_011535986.1:c.3588A>C	XP_011534288.1:p.Arg1196Ser
XM_011535987.1:c.3207A>C	XP_011534289.1:p.Arg1069Ser
XM_011535988.1:c.2070A>C	XP_011534290.1:p.Arg690Ser
NM_001346813.1:c.4929A>C	NP_001333742.1:p.Arg1643Ser
NM_001363725.1:c.2679A>C	NP_001350654.1:p.Arg893Ser
XM_011535984.2:c.5139A>C	XP_011534286.2:p.Arg1713Ser
XM_011535988.3:c.2070A>C	XP_011534290.1:p.Arg690Ser
XM_017011103.2:c.5040A>C	XP_016866592.1:p.Arg1680Ser
XM_017011104.1:c.5010A>C	XP_016866593.1:p.Arg1670Ser
XM_017011105.2:c.4980A>C	XP_016866594.1:p.Arg1660Ser
XM_017011106.2:c.4851A>C	XP_016866595.1:p.Arg1617Ser
XM_017011107.2:c.4830A>C	XP_016866596.1:p.Arg1610Ser
XR_002956289.1:n.5125A>C
NM_001363725.2:c.2679A>C	NP_001350654.1:p.Arg893Ser
NM_001371656.1:c.5058A>C	NP_001358585.1:p.Arg1686Ser
NM_001374820.1:c.5058A>C	NP_001361749.1:p.Arg1686Ser
NM_001374828.1:c.5178A>C MANE Select	NP_001361757.1:p.Arg1726Ser
NM_017519.3:c.5019A>C	NP_059989.3:p.Arg1673Ser