Canonical Allele Identifier: CA366227255

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502142A>G (hg19) ; chr6:g.157181008A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181008A>G , CM000668.2:g.157181008A>G	GRCh38
NC_000006.11:g.157502142A>G , CM000668.1:g.157502142A>G	GRCh37
NC_000006.10:g.157543834A>G	NCBI36
NG_032093.1:g.408079A>G
NG_032093.2:g.408079A>G
NG_066624.1:g.409983A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3385A>G	ENSP00000055163.8:p.Lys1129Glu
ENST00000414678.8:c.3454A>G	ENSP00000412835.3:p.Lys1152Glu
ENST00000637015.2:c.3673A>G	ENSP00000489729.2:p.Lys1225Glu
ENST00000319584.11:c.1558A>G	ENSP00000313006.7:p.Lys520Glu
ENST00000346085.10:c.3424A>G	ENSP00000344546.5:p.Lys1142Glu
ENST00000350026.10:c.3136A>G	ENSP00000055163.7:p.Lys1046Glu
ENST00000414678.7:c.1702A>G	ENSP00000412835.2:p.Lys568Glu
ENST00000635849.1:c.865A>G	ENSP00000490948.1:p.Lys289Glu
ENST00000635957.1:c.499A>G	ENSP00000490385.1:p.Lys167Glu
ENST00000636930.2:c.3544A>G MANE Select	ENSP00000490491.2:p.Lys1182Glu
ENST00000636940.1:n.1541A>G
ENST00000637015.1:c.912A>G
ENST00000637568.1:c.826A>G
ENST00000637741.1:n.210A>G
ENST00000637810.1:c.886A>G	ENSP00000489636.1:p.Lys296Glu
ENST00000637904.1:c.1045A>G	ENSP00000490550.1:p.Lys349Glu
ENST00000647938.1:c.3175A>G	ENSP00000498155.1:p.Lys1059Glu
ENST00000319584.10:c.1561A>G	ENSP00000313006.6:p.Lys521Glu
ENST00000346085.9:c.3175A>G	ENSP00000344546.4:p.Lys1059Glu
ENST00000350026.9:c.3136A>G	ENSP00000055163.7:p.Lys1046Glu
ENST00000400790.3:c.337A>G	ENSP00000383596.3:p.Lys113Glu
ENST00000414678.6:c.1702A>G	ENSP00000412835.2:p.Lys568Glu
ENST00000478761.3:c.746A>G
NM_017519.2:c.3136A>G	NP_059989.2:p.Lys1046Glu
NM_020732.3:c.3175A>G	NP_065783.3:p.Lys1059Glu
XM_005267069.3:c.3295A>G	XP_005267126.2:p.Lys1099Glu
XM_011535984.1:c.2374A>G	XP_011534286.1:p.Lys792Glu
XM_011535985.1:c.2194A>G	XP_011534287.1:p.Lys732Glu
XM_011535986.1:c.1954A>G	XP_011534288.1:p.Lys652Glu
XM_011535987.1:c.1573A>G	XP_011534289.1:p.Lys525Glu
XM_011535988.1:c.436A>G	XP_011534290.1:p.Lys146Glu
NM_001346813.1:c.3295A>G	NP_001333742.1:p.Lys1099Glu
NM_001363725.1:c.1045A>G	NP_001350654.1:p.Lys349Glu
XM_011535984.2:c.3505A>G	XP_011534286.2:p.Lys1169Glu
XM_011535988.3:c.436A>G	XP_011534290.1:p.Lys146Glu
XM_017011103.2:c.3406A>G	XP_016866592.1:p.Lys1136Glu
XM_017011104.1:c.3376A>G	XP_016866593.1:p.Lys1126Glu
XM_017011105.2:c.3346A>G	XP_016866594.1:p.Lys1116Glu
XM_017011106.2:c.3217A>G	XP_016866595.1:p.Lys1073Glu
XM_017011107.2:c.3196A>G	XP_016866596.1:p.Lys1066Glu
XR_002956289.1:n.3588A>G
NM_001363725.2:c.1045A>G	NP_001350654.1:p.Lys349Glu
NM_001371656.1:c.3424A>G	NP_001358585.1:p.Lys1142Glu
NM_001374820.1:c.3424A>G	NP_001361749.1:p.Lys1142Glu
NM_001374828.1:c.3544A>G MANE Select	NP_001361757.1:p.Lys1182Glu
NM_017519.3:c.3385A>G	NP_059989.3:p.Lys1129Glu