Canonical Allele Identifier: CA366234423

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510911G>C (hg19) ; chr6:g.157189777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189777G>C , CM000668.2:g.157189777G>C	GRCh38
NC_000006.11:g.157510911G>C , CM000668.1:g.157510911G>C	GRCh37
NC_000006.10:g.157552603G>C	NCBI36
NG_032093.1:g.416848G>C
NG_032093.2:g.416848G>C
NG_066624.1:g.418752G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3896G>C	ENSP00000055163.8:p.Gly1299Ala
ENST00000414678.8:c.3965G>C	ENSP00000412835.3:p.Gly1322Ala
ENST00000637015.2:c.4184G>C	ENSP00000489729.2:p.Gly1395Ala
ENST00000346085.10:c.3935G>C	ENSP00000344546.5:p.Gly1312Ala
ENST00000350026.10:c.3647G>C	ENSP00000055163.7:p.Gly1216Ala
ENST00000414678.7:c.2213G>C	ENSP00000412835.2:p.Gly738Ala
ENST00000635849.1:c.1376G>C	ENSP00000490948.1:p.Gly459Ala
ENST00000635957.1:c.1010G>C	ENSP00000490385.1:p.Gly337Ala
ENST00000636930.2:c.4055G>C MANE Select	ENSP00000490491.2:p.Gly1352Ala
ENST00000636940.1:n.2052G>C
ENST00000637015.1:c.1423G>C
ENST00000637568.1:c.1337G>C
ENST00000637741.1:n.721G>C
ENST00000637810.1:c.1397G>C	ENSP00000489636.1:p.Gly466Ala
ENST00000637904.1:c.1556G>C	ENSP00000490550.1:p.Gly519Ala
ENST00000647938.1:c.3686G>C	ENSP00000498155.1:p.Gly1229Ala
ENST00000346085.9:c.3686G>C	ENSP00000344546.4:p.Gly1229Ala
ENST00000350026.9:c.3647G>C	ENSP00000055163.7:p.Gly1216Ala
ENST00000414678.6:c.2213G>C	ENSP00000412835.2:p.Gly738Ala
NM_017519.2:c.3647G>C	NP_059989.2:p.Gly1216Ala
NM_020732.3:c.3686G>C	NP_065783.3:p.Gly1229Ala
XM_005267069.3:c.3806G>C	XP_005267126.2:p.Gly1269Ala
XM_011535984.1:c.2885G>C	XP_011534286.1:p.Gly962Ala
XM_011535985.1:c.2705G>C	XP_011534287.1:p.Gly902Ala
XM_011535986.1:c.2465G>C	XP_011534288.1:p.Gly822Ala
XM_011535987.1:c.2084G>C	XP_011534289.1:p.Gly695Ala
XM_011535988.1:c.947G>C	XP_011534290.1:p.Gly316Ala
NM_001346813.1:c.3806G>C	NP_001333742.1:p.Gly1269Ala
NM_001363725.1:c.1556G>C	NP_001350654.1:p.Gly519Ala
XM_011535984.2:c.4016G>C	XP_011534286.2:p.Gly1339Ala
XM_011535988.3:c.947G>C	XP_011534290.1:p.Gly316Ala
XM_017011103.2:c.3917G>C	XP_016866592.1:p.Gly1306Ala
XM_017011104.1:c.3887G>C	XP_016866593.1:p.Gly1296Ala
XM_017011105.2:c.3857G>C	XP_016866594.1:p.Gly1286Ala
XM_017011106.2:c.3728G>C	XP_016866595.1:p.Gly1243Ala
XM_017011107.2:c.3707G>C	XP_016866596.1:p.Gly1236Ala
XR_002956289.1:n.4099G>C
NM_001363725.2:c.1556G>C	NP_001350654.1:p.Gly519Ala
NM_001371656.1:c.3935G>C	NP_001358585.1:p.Gly1312Ala
NM_001374820.1:c.3935G>C	NP_001361749.1:p.Gly1312Ala
NM_001374828.1:c.4055G>C MANE Select	NP_001361757.1:p.Gly1352Ala
NM_017519.3:c.3896G>C	NP_059989.3:p.Gly1299Ala