Canonical Allele Identifier: CA366241621

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522167G>C (hg19) ; chr6:g.157201033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201033G>C , CM000668.2:g.157201033G>C	GRCh38
NC_000006.11:g.157522167G>C , CM000668.1:g.157522167G>C	GRCh37
NC_000006.10:g.157563859G>C	NCBI36
NG_032093.1:g.428104G>C
NG_032093.2:g.428104G>C
NG_066624.1:g.430008G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4649G>C	ENSP00000055163.8:p.Gly1550Ala
ENST00000414678.8:c.4718G>C	ENSP00000412835.3:p.Gly1573Ala
ENST00000637015.2:c.4937G>C	ENSP00000489729.2:p.Gly1646Ala
ENST00000346085.10:c.4688G>C	ENSP00000344546.5:p.Gly1563Ala
ENST00000350026.10:c.4400G>C	ENSP00000055163.7:p.Gly1467Ala
ENST00000414678.7:c.2966G>C	ENSP00000412835.2:p.Gly989Ala
ENST00000635849.1:c.2129G>C	ENSP00000490948.1:p.Gly710Ala
ENST00000635957.1:c.1760G>C	ENSP00000490385.1:p.Gly587Ala
ENST00000636227.1:n.3271G>C
ENST00000636254.1:n.728G>C
ENST00000636930.2:c.4808G>C MANE Select	ENSP00000490491.2:p.Gly1603Ala
ENST00000636940.1:n.2805G>C
ENST00000637015.1:c.2176G>C
ENST00000637568.1:c.2090G>C
ENST00000637741.1:n.1474G>C
ENST00000637810.1:c.2150G>C	ENSP00000489636.1:p.Gly717Ala
ENST00000637904.1:c.2309G>C	ENSP00000490550.1:p.Gly770Ala
ENST00000647938.1:c.4439G>C	ENSP00000498155.1:p.Gly1480Ala
ENST00000346085.9:c.4439G>C	ENSP00000344546.4:p.Gly1480Ala
ENST00000350026.9:c.4400G>C	ENSP00000055163.7:p.Gly1467Ala
ENST00000414678.6:c.2966G>C	ENSP00000412835.2:p.Gly989Ala
NM_017519.2:c.4400G>C	NP_059989.2:p.Gly1467Ala
NM_020732.3:c.4439G>C	NP_065783.3:p.Gly1480Ala
XM_005267069.3:c.4559G>C	XP_005267126.2:p.Gly1520Ala
XM_011535984.1:c.3638G>C	XP_011534286.1:p.Gly1213Ala
XM_011535985.1:c.3458G>C	XP_011534287.1:p.Gly1153Ala
XM_011535986.1:c.3218G>C	XP_011534288.1:p.Gly1073Ala
XM_011535987.1:c.2837G>C	XP_011534289.1:p.Gly946Ala
XM_011535988.1:c.1700G>C	XP_011534290.1:p.Gly567Ala
NM_001346813.1:c.4559G>C	NP_001333742.1:p.Gly1520Ala
NM_001363725.1:c.2309G>C	NP_001350654.1:p.Gly770Ala
XM_011535984.2:c.4769G>C	XP_011534286.2:p.Gly1590Ala
XM_011535988.3:c.1700G>C	XP_011534290.1:p.Gly567Ala
XM_017011103.2:c.4670G>C	XP_016866592.1:p.Gly1557Ala
XM_017011104.1:c.4640G>C	XP_016866593.1:p.Gly1547Ala
XM_017011105.2:c.4610G>C	XP_016866594.1:p.Gly1537Ala
XM_017011106.2:c.4481G>C	XP_016866595.1:p.Gly1494Ala
XM_017011107.2:c.4460G>C	XP_016866596.1:p.Gly1487Ala
XR_002956289.1:n.4755G>C
NM_001363725.2:c.2309G>C	NP_001350654.1:p.Gly770Ala
NM_001371656.1:c.4688G>C	NP_001358585.1:p.Gly1563Ala
NM_001374820.1:c.4688G>C	NP_001361749.1:p.Gly1563Ala
NM_001374828.1:c.4808G>C MANE Select	NP_001361757.1:p.Gly1603Ala
NM_017519.3:c.4649G>C	NP_059989.3:p.Gly1550Ala