Canonical Allele Identifier: CA366247100
Community Standard Title: NM_001374828.1(ARID1B):c.5896C>T (p.Arg1966Cys)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206668C>T , CM000668.2:g.157206668C>T GRCh38
NC_000006.11:g.157527802C>T , CM000668.1:g.157527802C>T GRCh37
NC_000006.10:g.157569494C>T NCBI36
NG_032093.1:g.433739C>T
NG_032093.2:g.433739C>T
NG_066624.1:g.435643C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.5896C>T MANE Select NP_001361757.1:p.Arg1966Cys
ENST00000636930.2:c.5896C>T MANE Select ENSP00000490491.2:p.Arg1966Cys
NM_001346813.1:c.5647C>T NP_001333742.1:p.Arg1883Cys
NM_001363725.1:c.3397C>T NP_001350654.1:p.Arg1133Cys
NM_001363725.2:c.3397C>T NP_001350654.1:p.Arg1133Cys
NM_001371656.1:c.5776C>T NP_001358585.1:p.Arg1926Cys
NM_001374820.1:c.5776C>T NP_001361749.1:p.Arg1926Cys
NM_017519.2:c.5488C>T NP_059989.2:p.Arg1830Cys
NM_017519.3:c.5737C>T NP_059989.3:p.Arg1913Cys
NM_020732.3:c.5527C>T NP_065783.3:p.Arg1843Cys
ENST00000346085.10:c.5776C>T ENSP00000344546.5:p.Arg1926Cys
ENST00000346085.9:c.5527C>T ENSP00000344546.4:p.Arg1843Cys
ENST00000350026.10:c.5488C>T ENSP00000055163.7:p.Arg1830Cys
ENST00000350026.11:c.5737C>T ENSP00000055163.8:p.Arg1913Cys
ENST00000350026.9:c.5488C>T ENSP00000055163.7:p.Arg1830Cys
ENST00000414678.6:c.4054C>T ENSP00000412835.2:p.Arg1352Cys
ENST00000414678.7:c.4054C>T ENSP00000412835.2:p.Arg1352Cys
ENST00000414678.8:c.5806C>T ENSP00000412835.3:p.Arg1936Cys
ENST00000635849.1:c.3217C>T ENSP00000490948.1:p.Arg1073Cys
ENST00000635928.1:c.52C>T ENSP00000489717.1:p.Arg18Cys
ENST00000635957.1:c.2848C>T ENSP00000490385.1:p.Arg950Cys
ENST00000636227.1:n.4359C>T
ENST00000636254.1:n.1816C>T
ENST00000636940.1:n.3893C>T
ENST00000637015.1:c.3264C>T
ENST00000637015.2:c.6025C>T ENSP00000489729.2:p.Arg2009Cys
ENST00000637568.1:c.3178C>T
ENST00000637741.1:n.2562C>T
ENST00000637810.1:c.3238C>T ENSP00000489636.1:p.Arg1080Cys
ENST00000637904.1:c.3397C>T ENSP00000490550.1:p.Arg1133Cys
ENST00000637933.1:n.3011C>T
ENST00000647938.1:c.5527C>T ENSP00000498155.1:p.Arg1843Cys
XM_005267069.3:c.5647C>T XP_005267126.2:p.Arg1883Cys
XM_011535984.1:c.4726C>T XP_011534286.1:p.Arg1576Cys
XM_011535984.2:c.5857C>T XP_011534286.2:p.Arg1953Cys
XM_011535985.1:c.4546C>T XP_011534287.1:p.Arg1516Cys
XM_011535986.1:c.4306C>T XP_011534288.1:p.Arg1436Cys
XM_011535987.1:c.3925C>T XP_011534289.1:p.Arg1309Cys
XM_011535988.1:c.2788C>T XP_011534290.1:p.Arg930Cys
XM_011535988.3:c.2788C>T XP_011534290.1:p.Arg930Cys
XM_017011103.2:c.5758C>T XP_016866592.1:p.Arg1920Cys
XM_017011104.1:c.5728C>T XP_016866593.1:p.Arg1910Cys
XM_017011105.2:c.5698C>T XP_016866594.1:p.Arg1900Cys
XM_017011106.2:c.5569C>T XP_016866595.1:p.Arg1857Cys
XM_017011107.2:c.5548C>T XP_016866596.1:p.Arg1850Cys
XR_002956289.1:n.5843C>T