Canonical Allele Identifier: CA366241800

Gene: ARID1B

Linked Data

• dbSNP Id: rs1274057762
• MyVariant Identifiers: chr6:g.157522202G>C (hg19) ; chr6:g.157201068G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201068G>C , CM000668.2:g.157201068G>C	GRCh38
NC_000006.11:g.157522202G>C , CM000668.1:g.157522202G>C	GRCh37
NC_000006.10:g.157563894G>C	NCBI36
NG_032093.1:g.428139G>C
NG_032093.2:g.428139G>C
NG_066624.1:g.430043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4684G>C	ENSP00000055163.8:p.Gly1562Arg
ENST00000414678.8:c.4753G>C	ENSP00000412835.3:p.Gly1585Arg
ENST00000637015.2:c.4972G>C	ENSP00000489729.2:p.Gly1658Arg
ENST00000346085.10:c.4723G>C	ENSP00000344546.5:p.Gly1575Arg
ENST00000350026.10:c.4435G>C	ENSP00000055163.7:p.Gly1479Arg
ENST00000414678.7:c.3001G>C	ENSP00000412835.2:p.Gly1001Arg
ENST00000635849.1:c.2164G>C	ENSP00000490948.1:p.Gly722Arg
ENST00000635957.1:c.1795G>C	ENSP00000490385.1:p.Gly599Arg
ENST00000636227.1:n.3306G>C
ENST00000636254.1:n.763G>C
ENST00000636930.2:c.4843G>C MANE Select	ENSP00000490491.2:p.Gly1615Arg
ENST00000636940.1:n.2840G>C
ENST00000637015.1:c.2211G>C
ENST00000637568.1:c.2125G>C
ENST00000637741.1:n.1509G>C
ENST00000637810.1:c.2185G>C	ENSP00000489636.1:p.Gly729Arg
ENST00000637904.1:c.2344G>C	ENSP00000490550.1:p.Gly782Arg
ENST00000647938.1:c.4474G>C	ENSP00000498155.1:p.Gly1492Arg
ENST00000346085.9:c.4474G>C	ENSP00000344546.4:p.Gly1492Arg
ENST00000350026.9:c.4435G>C	ENSP00000055163.7:p.Gly1479Arg
ENST00000414678.6:c.3001G>C	ENSP00000412835.2:p.Gly1001Arg
NM_017519.2:c.4435G>C	NP_059989.2:p.Gly1479Arg
NM_020732.3:c.4474G>C	NP_065783.3:p.Gly1492Arg
XM_005267069.3:c.4594G>C	XP_005267126.2:p.Gly1532Arg
XM_011535984.1:c.3673G>C	XP_011534286.1:p.Gly1225Arg
XM_011535985.1:c.3493G>C	XP_011534287.1:p.Gly1165Arg
XM_011535986.1:c.3253G>C	XP_011534288.1:p.Gly1085Arg
XM_011535987.1:c.2872G>C	XP_011534289.1:p.Gly958Arg
XM_011535988.1:c.1735G>C	XP_011534290.1:p.Gly579Arg
NM_001346813.1:c.4594G>C	NP_001333742.1:p.Gly1532Arg
NM_001363725.1:c.2344G>C	NP_001350654.1:p.Gly782Arg
XM_011535984.2:c.4804G>C	XP_011534286.2:p.Gly1602Arg
XM_011535988.3:c.1735G>C	XP_011534290.1:p.Gly579Arg
XM_017011103.2:c.4705G>C	XP_016866592.1:p.Gly1569Arg
XM_017011104.1:c.4675G>C	XP_016866593.1:p.Gly1559Arg
XM_017011105.2:c.4645G>C	XP_016866594.1:p.Gly1549Arg
XM_017011106.2:c.4516G>C	XP_016866595.1:p.Gly1506Arg
XM_017011107.2:c.4495G>C	XP_016866596.1:p.Gly1499Arg
XR_002956289.1:n.4790G>C
NM_001363725.2:c.2344G>C	NP_001350654.1:p.Gly782Arg
NM_001371656.1:c.4723G>C	NP_001358585.1:p.Gly1575Arg
NM_001374820.1:c.4723G>C	NP_001361749.1:p.Gly1575Arg
NM_001374828.1:c.4843G>C MANE Select	NP_001361757.1:p.Gly1615Arg
NM_017519.3:c.4684G>C	NP_059989.3:p.Gly1562Arg