Canonical Allele Identifier: CA366239788

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157520009G>C (hg19) ; chr6:g.157198875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198875G>C , CM000668.2:g.157198875G>C	GRCh38
NC_000006.11:g.157520009G>C , CM000668.1:g.157520009G>C	GRCh37
NC_000006.10:g.157561701G>C	NCBI36
NG_032093.1:g.425946G>C
NG_032093.2:g.425946G>C
NG_066624.1:g.427850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4288G>C	ENSP00000055163.8:p.Gly1430Arg
ENST00000414678.8:c.4357G>C	ENSP00000412835.3:p.Gly1453Arg
ENST00000637015.2:c.4576G>C	ENSP00000489729.2:p.Gly1526Arg
ENST00000346085.10:c.4327G>C	ENSP00000344546.5:p.Gly1443Arg
ENST00000350026.10:c.4039G>C	ENSP00000055163.7:p.Gly1347Arg
ENST00000414678.7:c.2605G>C	ENSP00000412835.2:p.Gly869Arg
ENST00000635849.1:c.1768G>C	ENSP00000490948.1:p.Gly590Arg
ENST00000635957.1:c.1399G>C	ENSP00000490385.1:p.Gly467Arg
ENST00000636227.1:n.2910G>C
ENST00000636254.1:n.367G>C
ENST00000636930.2:c.4447G>C MANE Select	ENSP00000490491.2:p.Gly1483Arg
ENST00000636940.1:n.2444G>C
ENST00000637015.1:c.1815G>C
ENST00000637568.1:c.1729G>C
ENST00000637741.1:n.1113G>C
ENST00000637810.1:c.1789G>C	ENSP00000489636.1:p.Gly597Arg
ENST00000637904.1:c.1948G>C	ENSP00000490550.1:p.Gly650Arg
ENST00000647938.1:c.4078G>C	ENSP00000498155.1:p.Gly1360Arg
ENST00000346085.9:c.4078G>C	ENSP00000344546.4:p.Gly1360Arg
ENST00000350026.9:c.4039G>C	ENSP00000055163.7:p.Gly1347Arg
ENST00000414678.6:c.2605G>C	ENSP00000412835.2:p.Gly869Arg
NM_017519.2:c.4039G>C	NP_059989.2:p.Gly1347Arg
NM_020732.3:c.4078G>C	NP_065783.3:p.Gly1360Arg
XM_005267069.3:c.4198G>C	XP_005267126.2:p.Gly1400Arg
XM_011535984.1:c.3277G>C	XP_011534286.1:p.Gly1093Arg
XM_011535985.1:c.3097G>C	XP_011534287.1:p.Gly1033Arg
XM_011535986.1:c.2857G>C	XP_011534288.1:p.Gly953Arg
XM_011535987.1:c.2476G>C	XP_011534289.1:p.Gly826Arg
XM_011535988.1:c.1339G>C	XP_011534290.1:p.Gly447Arg
NM_001346813.1:c.4198G>C	NP_001333742.1:p.Gly1400Arg
NM_001363725.1:c.1948G>C	NP_001350654.1:p.Gly650Arg
XM_011535984.2:c.4408G>C	XP_011534286.2:p.Gly1470Arg
XM_011535988.3:c.1339G>C	XP_011534290.1:p.Gly447Arg
XM_017011103.2:c.4309G>C	XP_016866592.1:p.Gly1437Arg
XM_017011104.1:c.4279G>C	XP_016866593.1:p.Gly1427Arg
XM_017011105.2:c.4249G>C	XP_016866594.1:p.Gly1417Arg
XM_017011106.2:c.4120G>C	XP_016866595.1:p.Gly1374Arg
XM_017011107.2:c.4099G>C	XP_016866596.1:p.Gly1367Arg
XR_002956289.1:n.4427-1830G>C
NM_001363725.2:c.1948G>C	NP_001350654.1:p.Gly650Arg
NM_001371656.1:c.4327G>C	NP_001358585.1:p.Gly1443Arg
NM_001374820.1:c.4327G>C	NP_001361749.1:p.Gly1443Arg
NM_001374828.1:c.4447G>C MANE Select	NP_001361757.1:p.Gly1483Arg
NM_017519.3:c.4288G>C	NP_059989.3:p.Gly1430Arg