Canonical Allele Identifier: CA366230222
Community Standard Title: NM_001374828.1(ARID1B):c.3770C>G (p.Ser1257Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184286C>G , CM000668.2:g.157184286C>G GRCh38
NC_000006.11:g.157505420C>G , CM000668.1:g.157505420C>G GRCh37
NC_000006.10:g.157547112C>G NCBI36
NG_032093.1:g.411357C>G
NG_032093.2:g.411357C>G
NG_066624.1:g.413261C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3770C>G MANE Select NP_001361757.1:p.Ser1257Ter
ENST00000636930.2:c.3770C>G MANE Select ENSP00000490491.2:p.Ser1257Ter
NM_001346813.1:c.3521C>G NP_001333742.1:p.Ser1174Ter
NM_001363725.1:c.1271C>G NP_001350654.1:p.Ser424Ter
NM_001363725.2:c.1271C>G NP_001350654.1:p.Ser424Ter
NM_001371656.1:c.3650C>G NP_001358585.1:p.Ser1217Ter
NM_001374820.1:c.3650C>G NP_001361749.1:p.Ser1217Ter
NM_017519.2:c.3362C>G NP_059989.2:p.Ser1121Ter
NM_017519.3:c.3611C>G NP_059989.3:p.Ser1204Ter
NM_020732.3:c.3401C>G NP_065783.3:p.Ser1134Ter
ENST00000319584.10:c.1787C>G ENSP00000313006.6:p.Ser596Ter
ENST00000319584.11:c.1784C>G ENSP00000313006.7:p.Ser595Ter
ENST00000346085.10:c.3650C>G ENSP00000344546.5:p.Ser1217Ter
ENST00000346085.9:c.3401C>G ENSP00000344546.4:p.Ser1134Ter
ENST00000350026.10:c.3362C>G ENSP00000055163.7:p.Ser1121Ter
ENST00000350026.11:c.3611C>G ENSP00000055163.8:p.Ser1204Ter
ENST00000350026.9:c.3362C>G ENSP00000055163.7:p.Ser1121Ter
ENST00000400790.3:c.563C>G ENSP00000383596.3:p.Ser188Ter
ENST00000414678.6:c.1928C>G ENSP00000412835.2:p.Ser643Ter
ENST00000414678.7:c.1928C>G ENSP00000412835.2:p.Ser643Ter
ENST00000414678.8:c.3680C>G ENSP00000412835.3:p.Ser1227Ter
ENST00000635849.1:c.1091C>G ENSP00000490948.1:p.Ser364Ter
ENST00000635957.1:c.725C>G ENSP00000490385.1:p.Ser242Ter
ENST00000636940.1:n.1767C>G
ENST00000637015.1:c.1138C>G
ENST00000637015.2:c.3899C>G ENSP00000489729.2:p.Ser1300Ter
ENST00000637568.1:c.1052C>G
ENST00000637741.1:n.436C>G
ENST00000637810.1:c.1112C>G ENSP00000489636.1:p.Ser371Ter
ENST00000637904.1:c.1271C>G ENSP00000490550.1:p.Ser424Ter
ENST00000647938.1:c.3401C>G ENSP00000498155.1:p.Ser1134Ter
XM_005267069.3:c.3521C>G XP_005267126.2:p.Ser1174Ter
XM_011535984.1:c.2600C>G XP_011534286.1:p.Ser867Ter
XM_011535984.2:c.3731C>G XP_011534286.2:p.Ser1244Ter
XM_011535985.1:c.2420C>G XP_011534287.1:p.Ser807Ter
XM_011535986.1:c.2180C>G XP_011534288.1:p.Ser727Ter
XM_011535987.1:c.1799C>G XP_011534289.1:p.Ser600Ter
XM_011535988.1:c.662C>G XP_011534290.1:p.Ser221Ter
XM_011535988.3:c.662C>G XP_011534290.1:p.Ser221Ter
XM_017011103.2:c.3632C>G XP_016866592.1:p.Ser1211Ter
XM_017011104.1:c.3602C>G XP_016866593.1:p.Ser1201Ter
XM_017011105.2:c.3572C>G XP_016866594.1:p.Ser1191Ter
XM_017011106.2:c.3443C>G XP_016866595.1:p.Ser1148Ter
XM_017011107.2:c.3422C>G XP_016866596.1:p.Ser1141Ter
XR_002956289.1:n.3814C>G