Canonical Allele Identifier: CA4067664
Community Standard Title: NM_001374828.1(ARID1B):c.4609C>G (p.Pro1537Ala)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200834C>G , CM000668.2:g.157200834C>G GRCh38
NC_000006.11:g.157521968C>G , CM000668.1:g.157521968C>G GRCh37
NC_000006.10:g.157563660C>G NCBI36
NG_032093.1:g.427905C>G
NG_032093.2:g.427905C>G
NG_066624.1:g.429809C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.4609C>G MANE Select NP_001361757.1:p.Pro1537Ala
ENST00000636930.2:c.4609C>G MANE Select ENSP00000490491.2:p.Pro1537Ala
NM_001346813.1:c.4360C>G NP_001333742.1:p.Pro1454Ala
NM_001363725.1:c.2110C>G NP_001350654.1:p.Pro704Ala
NM_001363725.2:c.2110C>G NP_001350654.1:p.Pro704Ala
NM_001371656.1:c.4489C>G NP_001358585.1:p.Pro1497Ala
NM_001374820.1:c.4489C>G NP_001361749.1:p.Pro1497Ala
NM_017519.2:c.4201C>G NP_059989.2:p.Pro1401Ala
NM_017519.3:c.4450C>G NP_059989.3:p.Pro1484Ala
NM_020732.3:c.4240C>G NP_065783.3:p.Pro1414Ala
ENST00000346085.10:c.4489C>G ENSP00000344546.5:p.Pro1497Ala
ENST00000346085.9:c.4240C>G ENSP00000344546.4:p.Pro1414Ala
ENST00000350026.10:c.4201C>G ENSP00000055163.7:p.Pro1401Ala
ENST00000350026.11:c.4450C>G ENSP00000055163.8:p.Pro1484Ala
ENST00000350026.9:c.4201C>G ENSP00000055163.7:p.Pro1401Ala
ENST00000414678.6:c.2767C>G ENSP00000412835.2:p.Pro923Ala
ENST00000414678.7:c.2767C>G ENSP00000412835.2:p.Pro923Ala
ENST00000414678.8:c.4519C>G ENSP00000412835.3:p.Pro1507Ala
ENST00000635849.1:c.1930C>G ENSP00000490948.1:p.Pro644Ala
ENST00000635957.1:c.1561C>G ENSP00000490385.1:p.Pro521Ala
ENST00000636227.1:n.3072C>G
ENST00000636254.1:n.529C>G
ENST00000636940.1:n.2606C>G
ENST00000637015.1:c.1977C>G
ENST00000637015.2:c.4738C>G ENSP00000489729.2:p.Pro1580Ala
ENST00000637568.1:c.1891C>G
ENST00000637741.1:n.1275C>G
ENST00000637810.1:c.1951C>G ENSP00000489636.1:p.Pro651Ala
ENST00000637904.1:c.2110C>G ENSP00000490550.1:p.Pro704Ala
ENST00000647938.1:c.4240C>G ENSP00000498155.1:p.Pro1414Ala
XM_005267069.3:c.4360C>G XP_005267126.2:p.Pro1454Ala
XM_011535984.1:c.3439C>G XP_011534286.1:p.Pro1147Ala
XM_011535984.2:c.4570C>G XP_011534286.2:p.Pro1524Ala
XM_011535985.1:c.3259C>G XP_011534287.1:p.Pro1087Ala
XM_011535986.1:c.3019C>G XP_011534288.1:p.Pro1007Ala
XM_011535987.1:c.2638C>G XP_011534289.1:p.Pro880Ala
XM_011535988.1:c.1501C>G XP_011534290.1:p.Pro501Ala
XM_011535988.3:c.1501C>G XP_011534290.1:p.Pro501Ala
XM_017011103.2:c.4471C>G XP_016866592.1:p.Pro1491Ala
XM_017011104.1:c.4441C>G XP_016866593.1:p.Pro1481Ala
XM_017011105.2:c.4411C>G XP_016866594.1:p.Pro1471Ala
XM_017011106.2:c.4282C>G XP_016866595.1:p.Pro1428Ala
XM_017011107.2:c.4261C>G XP_016866596.1:p.Pro1421Ala
XR_002956289.1:n.4556C>G