Canonical Allele Identifier: CA366242104

Gene: ARID1B

Linked Data

• dbSNP Id: rs1263274493
• MyVariant Identifiers: chr6:g.157522279C>G (hg19) ; chr6:g.157201145C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201145C>G , CM000668.2:g.157201145C>G	GRCh38
NC_000006.11:g.157522279C>G , CM000668.1:g.157522279C>G	GRCh37
NC_000006.10:g.157563971C>G	NCBI36
NG_032093.1:g.428216C>G
NG_032093.2:g.428216C>G
NG_066624.1:g.430120C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4761C>G	ENSP00000055163.8:p.Ser1587Arg
ENST00000414678.8:c.4830C>G	ENSP00000412835.3:p.Ser1610Arg
ENST00000637015.2:c.5049C>G	ENSP00000489729.2:p.Ser1683Arg
ENST00000346085.10:c.4800C>G	ENSP00000344546.5:p.Ser1600Arg
ENST00000350026.10:c.4512C>G	ENSP00000055163.7:p.Ser1504Arg
ENST00000414678.7:c.3078C>G	ENSP00000412835.2:p.Ser1026Arg
ENST00000635849.1:c.2241C>G	ENSP00000490948.1:p.Ser747Arg
ENST00000635957.1:c.1872C>G	ENSP00000490385.1:p.Ser624Arg
ENST00000636227.1:n.3383C>G
ENST00000636254.1:n.840C>G
ENST00000636930.2:c.4920C>G MANE Select	ENSP00000490491.2:p.Ser1640Arg
ENST00000636940.1:n.2917C>G
ENST00000637015.1:c.2288C>G
ENST00000637568.1:c.2202C>G
ENST00000637741.1:n.1586C>G
ENST00000637810.1:c.2262C>G	ENSP00000489636.1:p.Ser754Arg
ENST00000637904.1:c.2421C>G	ENSP00000490550.1:p.Ser807Arg
ENST00000647938.1:c.4551C>G	ENSP00000498155.1:p.Ser1517Arg
ENST00000346085.9:c.4551C>G	ENSP00000344546.4:p.Ser1517Arg
ENST00000350026.9:c.4512C>G	ENSP00000055163.7:p.Ser1504Arg
ENST00000414678.6:c.3078C>G	ENSP00000412835.2:p.Ser1026Arg
NM_017519.2:c.4512C>G	NP_059989.2:p.Ser1504Arg
NM_020732.3:c.4551C>G	NP_065783.3:p.Ser1517Arg
XM_005267069.3:c.4671C>G	XP_005267126.2:p.Ser1557Arg
XM_011535984.1:c.3750C>G	XP_011534286.1:p.Ser1250Arg
XM_011535985.1:c.3570C>G	XP_011534287.1:p.Ser1190Arg
XM_011535986.1:c.3330C>G	XP_011534288.1:p.Ser1110Arg
XM_011535987.1:c.2949C>G	XP_011534289.1:p.Ser983Arg
XM_011535988.1:c.1812C>G	XP_011534290.1:p.Ser604Arg
NM_001346813.1:c.4671C>G	NP_001333742.1:p.Ser1557Arg
NM_001363725.1:c.2421C>G	NP_001350654.1:p.Ser807Arg
XM_011535984.2:c.4881C>G	XP_011534286.2:p.Ser1627Arg
XM_011535988.3:c.1812C>G	XP_011534290.1:p.Ser604Arg
XM_017011103.2:c.4782C>G	XP_016866592.1:p.Ser1594Arg
XM_017011104.1:c.4752C>G	XP_016866593.1:p.Ser1584Arg
XM_017011105.2:c.4722C>G	XP_016866594.1:p.Ser1574Arg
XM_017011106.2:c.4593C>G	XP_016866595.1:p.Ser1531Arg
XM_017011107.2:c.4572C>G	XP_016866596.1:p.Ser1524Arg
XR_002956289.1:n.4867C>G
NM_001363725.2:c.2421C>G	NP_001350654.1:p.Ser807Arg
NM_001371656.1:c.4800C>G	NP_001358585.1:p.Ser1600Arg
NM_001374820.1:c.4800C>G	NP_001361749.1:p.Ser1600Arg
NM_001374828.1:c.4920C>G MANE Select	NP_001361757.1:p.Ser1640Arg
NM_017519.3:c.4761C>G	NP_059989.3:p.Ser1587Arg