Canonical Allele Identifier: CA366245893
Community Standard Title: NM_001374828.1(ARID1B):c.5570A>G (p.Asp1857Gly)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206342A>G , CM000668.2:g.157206342A>G GRCh38
NC_000006.11:g.157527476A>G , CM000668.1:g.157527476A>G GRCh37
NC_000006.10:g.157569168A>G NCBI36
NG_032093.1:g.433413A>G
NG_032093.2:g.433413A>G
NG_066624.1:g.435317A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.5570A>G MANE Select NP_001361757.1:p.Asp1857Gly
ENST00000636930.2:c.5570A>G MANE Select ENSP00000490491.2:p.Asp1857Gly
NM_001346813.1:c.5321A>G NP_001333742.1:p.Asp1774Gly
NM_001363725.1:c.3071A>G NP_001350654.1:p.Asp1024Gly
NM_001363725.2:c.3071A>G NP_001350654.1:p.Asp1024Gly
NM_001371656.1:c.5450A>G NP_001358585.1:p.Asp1817Gly
NM_001374820.1:c.5450A>G NP_001361749.1:p.Asp1817Gly
NM_017519.2:c.5162A>G NP_059989.2:p.Asp1721Gly
NM_017519.3:c.5411A>G NP_059989.3:p.Asp1804Gly
NM_020732.3:c.5201A>G NP_065783.3:p.Asp1734Gly
ENST00000346085.10:c.5450A>G ENSP00000344546.5:p.Asp1817Gly
ENST00000346085.9:c.5201A>G ENSP00000344546.4:p.Asp1734Gly
ENST00000350026.10:c.5162A>G ENSP00000055163.7:p.Asp1721Gly
ENST00000350026.11:c.5411A>G ENSP00000055163.8:p.Asp1804Gly
ENST00000350026.9:c.5162A>G ENSP00000055163.7:p.Asp1721Gly
ENST00000414678.6:c.3728A>G ENSP00000412835.2:p.Asp1243Gly
ENST00000414678.7:c.3728A>G ENSP00000412835.2:p.Asp1243Gly
ENST00000414678.8:c.5480A>G ENSP00000412835.3:p.Asp1827Gly
ENST00000635849.1:c.2891A>G ENSP00000490948.1:p.Asp964Gly
ENST00000635957.1:c.2522A>G ENSP00000490385.1:p.Asp841Gly
ENST00000636227.1:n.4033A>G
ENST00000636254.1:n.1490A>G
ENST00000636940.1:n.3567A>G
ENST00000637015.1:c.2938A>G
ENST00000637015.2:c.5699A>G ENSP00000489729.2:p.Asp1900Gly
ENST00000637568.1:c.2852A>G
ENST00000637741.1:n.2236A>G
ENST00000637810.1:c.2912A>G ENSP00000489636.1:p.Asp971Gly
ENST00000637904.1:c.3071A>G ENSP00000490550.1:p.Asp1024Gly
ENST00000637933.1:n.2685A>G
ENST00000647938.1:c.5201A>G ENSP00000498155.1:p.Asp1734Gly
XM_005267069.3:c.5321A>G XP_005267126.2:p.Asp1774Gly
XM_011535984.1:c.4400A>G XP_011534286.1:p.Asp1467Gly
XM_011535984.2:c.5531A>G XP_011534286.2:p.Asp1844Gly
XM_011535985.1:c.4220A>G XP_011534287.1:p.Asp1407Gly
XM_011535986.1:c.3980A>G XP_011534288.1:p.Asp1327Gly
XM_011535987.1:c.3599A>G XP_011534289.1:p.Asp1200Gly
XM_011535988.1:c.2462A>G XP_011534290.1:p.Asp821Gly
XM_011535988.3:c.2462A>G XP_011534290.1:p.Asp821Gly
XM_017011103.2:c.5432A>G XP_016866592.1:p.Asp1811Gly
XM_017011104.1:c.5402A>G XP_016866593.1:p.Asp1801Gly
XM_017011105.2:c.5372A>G XP_016866594.1:p.Asp1791Gly
XM_017011106.2:c.5243A>G XP_016866595.1:p.Asp1748Gly
XM_017011107.2:c.5222A>G XP_016866596.1:p.Asp1741Gly
XR_002956289.1:n.5517A>G