Canonical Allele Identifier: CA821320520

Gene: ARID1B

Linked Data

• dbSNP Id: rs1396649736
• gnomAD v4: 6-157189896-G-C
• MyVariant Identifiers: chr6:g.157511030G>C (hg19) ; chr6:g.157189896G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189896G>C , CM000668.2:g.157189896G>C	GRCh38
NC_000006.11:g.157511030G>C , CM000668.1:g.157511030G>C	GRCh37
NC_000006.10:g.157552722G>C	NCBI36
NG_032093.1:g.416967G>C
NG_032093.2:g.416967G>C
NG_066624.1:g.418871G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3899+116G>C	ENSP00000055163.8:n.3899+116G>C
ENST00000414678.8:c.3968+116G>C	ENSP00000412835.3:n.3968+116G>C
ENST00000637015.2:c.4187+116G>C	ENSP00000489729.2:n.4187+116G>C
ENST00000346085.10:c.3938+116G>C	ENSP00000344546.5:n.3938+116G>C
ENST00000350026.10:c.3650+116G>C	ENSP00000055163.7:n.3650+116G>C
ENST00000414678.7:c.2216+116G>C	ENSP00000412835.2:n.2216+116G>C
ENST00000635849.1:c.1379+116G>C	ENSP00000490948.1:n.1379+116G>C
ENST00000635957.1:c.1013+116G>C	ENSP00000490385.1:n.1013+116G>C
ENST00000636930.2:c.4058+116G>C MANE Select	ENSP00000490491.2:n.4058+116G>C
ENST00000636940.1:n.2055+116G>C
ENST00000637015.1:c.1426+116G>C
ENST00000637568.1:c.1340+116G>C
ENST00000637741.1:n.724+116G>C
ENST00000637810.1:c.1400+116G>C	ENSP00000489636.1:n.1400+116G>C
ENST00000637904.1:c.1559+116G>C	ENSP00000490550.1:n.1559+116G>C
ENST00000647938.1:c.3689+116G>C	ENSP00000498155.1:n.3689+116G>C
ENST00000346085.9:c.3689+116G>C	ENSP00000344546.4:n.3689+116G>C
ENST00000350026.9:c.3650+116G>C	ENSP00000055163.7:n.3650+116G>C
ENST00000414678.6:c.2216+116G>C	ENSP00000412835.2:n.2216+116G>C
NM_017519.2:c.3650+116G>C	NP_059989.2:n.3650+116G>C
NM_020732.3:c.3689+116G>C	NP_065783.3:n.3689+116G>C
XM_005267069.3:c.3809+116G>C	XP_005267126.2:n.3809+116G>C
XM_011535984.1:c.2888+116G>C	XP_011534286.1:n.2888+116G>C
XM_011535985.1:c.2708+116G>C	XP_011534287.1:n.2708+116G>C
XM_011535986.1:c.2468+116G>C	XP_011534288.1:n.2468+116G>C
XM_011535987.1:c.2087+116G>C	XP_011534289.1:n.2087+116G>C
XM_011535988.1:c.950+116G>C	XP_011534290.1:n.950+116G>C
NM_001346813.1:c.3809+116G>C	NP_001333742.1:n.3809+116G>C
NM_001363725.1:c.1559+116G>C	NP_001350654.1:n.1559+116G>C
XM_011535984.2:c.4019+116G>C	XP_011534286.2:n.4019+116G>C
XM_011535988.3:c.950+116G>C	XP_011534290.1:n.950+116G>C
XM_017011103.2:c.3920+116G>C	XP_016866592.1:n.3920+116G>C
XM_017011104.1:c.3890+116G>C	XP_016866593.1:n.3890+116G>C
XM_017011105.2:c.3860+116G>C	XP_016866594.1:n.3860+116G>C
XM_017011106.2:c.3731+116G>C	XP_016866595.1:n.3731+116G>C
XM_017011107.2:c.3710+116G>C	XP_016866596.1:n.3710+116G>C
XR_002956289.1:n.4102+116G>C
NM_001363725.2:c.1559+116G>C	NP_001350654.1:n.1559+116G>C
NM_001371656.1:c.3938+116G>C	NP_001358585.1:n.3938+116G>C
NM_001374820.1:c.3938+116G>C	NP_001361749.1:n.3938+116G>C
NM_001374828.1:c.4058+116G>C MANE Select	NP_001361757.1:n.4058+116G>C
NM_017519.3:c.3899+116G>C	NP_059989.3:n.3899+116G>C