Canonical Allele Identifier: CA366241744

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374252
• MyVariant Identifiers: chr6:g.157522191C>G (hg19) ; chr6:g.157201057C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201057C>G , CM000668.2:g.157201057C>G	GRCh38
NC_000006.11:g.157522191C>G , CM000668.1:g.157522191C>G	GRCh37
NC_000006.10:g.157563883C>G	NCBI36
NG_032093.1:g.428128C>G
NG_032093.2:g.428128C>G
NG_066624.1:g.430032C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4673C>G	ENSP00000055163.8:p.Pro1558Arg
ENST00000414678.8:c.4742C>G	ENSP00000412835.3:p.Pro1581Arg
ENST00000637015.2:c.4961C>G	ENSP00000489729.2:p.Pro1654Arg
ENST00000346085.10:c.4712C>G	ENSP00000344546.5:p.Pro1571Arg
ENST00000350026.10:c.4424C>G	ENSP00000055163.7:p.Pro1475Arg
ENST00000414678.7:c.2990C>G	ENSP00000412835.2:p.Pro997Arg
ENST00000635849.1:c.2153C>G	ENSP00000490948.1:p.Pro718Arg
ENST00000635957.1:c.1784C>G	ENSP00000490385.1:p.Pro595Arg
ENST00000636227.1:n.3295C>G
ENST00000636254.1:n.752C>G
ENST00000636930.2:c.4832C>G MANE Select	ENSP00000490491.2:p.Pro1611Arg
ENST00000636940.1:n.2829C>G
ENST00000637015.1:c.2200C>G
ENST00000637568.1:c.2114C>G
ENST00000637741.1:n.1498C>G
ENST00000637810.1:c.2174C>G	ENSP00000489636.1:p.Pro725Arg
ENST00000637904.1:c.2333C>G	ENSP00000490550.1:p.Pro778Arg
ENST00000647938.1:c.4463C>G	ENSP00000498155.1:p.Pro1488Arg
ENST00000346085.9:c.4463C>G	ENSP00000344546.4:p.Pro1488Arg
ENST00000350026.9:c.4424C>G	ENSP00000055163.7:p.Pro1475Arg
ENST00000414678.6:c.2990C>G	ENSP00000412835.2:p.Pro997Arg
NM_017519.2:c.4424C>G	NP_059989.2:p.Pro1475Arg
NM_020732.3:c.4463C>G	NP_065783.3:p.Pro1488Arg
XM_005267069.3:c.4583C>G	XP_005267126.2:p.Pro1528Arg
XM_011535984.1:c.3662C>G	XP_011534286.1:p.Pro1221Arg
XM_011535985.1:c.3482C>G	XP_011534287.1:p.Pro1161Arg
XM_011535986.1:c.3242C>G	XP_011534288.1:p.Pro1081Arg
XM_011535987.1:c.2861C>G	XP_011534289.1:p.Pro954Arg
XM_011535988.1:c.1724C>G	XP_011534290.1:p.Pro575Arg
NM_001346813.1:c.4583C>G	NP_001333742.1:p.Pro1528Arg
NM_001363725.1:c.2333C>G	NP_001350654.1:p.Pro778Arg
XM_011535984.2:c.4793C>G	XP_011534286.2:p.Pro1598Arg
XM_011535988.3:c.1724C>G	XP_011534290.1:p.Pro575Arg
XM_017011103.2:c.4694C>G	XP_016866592.1:p.Pro1565Arg
XM_017011104.1:c.4664C>G	XP_016866593.1:p.Pro1555Arg
XM_017011105.2:c.4634C>G	XP_016866594.1:p.Pro1545Arg
XM_017011106.2:c.4505C>G	XP_016866595.1:p.Pro1502Arg
XM_017011107.2:c.4484C>G	XP_016866596.1:p.Pro1495Arg
XR_002956289.1:n.4779C>G
NM_001363725.2:c.2333C>G	NP_001350654.1:p.Pro778Arg
NM_001371656.1:c.4712C>G	NP_001358585.1:p.Pro1571Arg
NM_001374820.1:c.4712C>G	NP_001361749.1:p.Pro1571Arg
NM_001374828.1:c.4832C>G MANE Select	NP_001361757.1:p.Pro1611Arg
NM_017519.3:c.4673C>G	NP_059989.3:p.Pro1558Arg