Canonical Allele Identifier: CA366237824
Community Standard Title: NM_001374828.1(ARID1B):c.4232-1G>A
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157196164G>A , CM000668.2:g.157196164G>A GRCh38
NC_000006.11:g.157517298G>A , CM000668.1:g.157517298G>A GRCh37
NC_000006.10:g.157558990G>A NCBI36
NG_032093.1:g.423235G>A
NG_032093.2:g.423235G>A
NG_066624.1:g.425139G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.4232-1G>A MANE Select NP_001361757.1:n.4232-1G>A
ENST00000636930.2:c.4232-1G>A MANE Select ENSP00000490491.2:n.4232-1G>A
NM_001346813.1:c.3983-1G>A NP_001333742.1:n.3983-1G>A
NM_001363725.1:c.1733-1G>A NP_001350654.1:n.1733-1G>A
NM_001363725.2:c.1733-1G>A NP_001350654.1:n.1733-1G>A
NM_001371656.1:c.4112-1G>A NP_001358585.1:n.4112-1G>A
NM_001374820.1:c.4112-1G>A NP_001361749.1:n.4112-1G>A
NM_017519.2:c.3824-1G>A NP_059989.2:n.3824-1G>A
NM_017519.3:c.4073-1G>A NP_059989.3:n.4073-1G>A
NM_020732.3:c.3863-1G>A NP_065783.3:n.3863-1G>A
ENST00000346085.10:c.4112-1G>A ENSP00000344546.5:n.4112-1G>A
ENST00000346085.9:c.3863-1G>A ENSP00000344546.4:n.3863-1G>A
ENST00000350026.10:c.3824-1G>A ENSP00000055163.7:n.3824-1G>A
ENST00000350026.11:c.4073-1G>A ENSP00000055163.8:n.4073-1G>A
ENST00000350026.9:c.3824-1G>A ENSP00000055163.7:n.3824-1G>A
ENST00000414678.6:c.2390-1G>A ENSP00000412835.2:n.2390-1G>A
ENST00000414678.7:c.2390-1G>A ENSP00000412835.2:n.2390-1G>A
ENST00000414678.8:c.4142-1G>A ENSP00000412835.3:n.4142-1G>A
ENST00000635849.1:c.1553-1G>A ENSP00000490948.1:n.1553-1G>A
ENST00000635957.1:c.1184-1G>A ENSP00000490385.1:n.1184-1G>A
ENST00000636227.1:n.2694G>A
ENST00000636940.1:n.2229-1G>A
ENST00000637015.1:c.1600-1G>A
ENST00000637015.2:c.4361-1G>A ENSP00000489729.2:n.4361-1G>A
ENST00000637568.1:c.1514-1G>A
ENST00000637741.1:n.898-1G>A
ENST00000637810.1:c.1574-1G>A ENSP00000489636.1:n.1574-1G>A
ENST00000637904.1:c.1733-1G>A ENSP00000490550.1:n.1733-1G>A
ENST00000647938.1:c.3863-1G>A ENSP00000498155.1:n.3863-1G>A
XM_005267069.3:c.3983-1G>A XP_005267126.2:n.3983-1G>A
XM_011535984.1:c.3062-1G>A XP_011534286.1:n.3062-1G>A
XM_011535984.2:c.4193-1G>A XP_011534286.2:n.4193-1G>A
XM_011535985.1:c.2882-1G>A XP_011534287.1:n.2882-1G>A
XM_011535986.1:c.2642-1G>A XP_011534288.1:n.2642-1G>A
XM_011535987.1:c.2261-1G>A XP_011534289.1:n.2261-1G>A
XM_011535988.1:c.1124-1G>A XP_011534290.1:n.1124-1G>A
XM_011535988.3:c.1124-1G>A XP_011534290.1:n.1124-1G>A
XM_017011103.2:c.4094-1G>A XP_016866592.1:n.4094-1G>A
XM_017011104.1:c.4064-1G>A XP_016866593.1:n.4064-1G>A
XM_017011105.2:c.4034-1G>A XP_016866594.1:n.4034-1G>A
XM_017011106.2:c.3905-1G>A XP_016866595.1:n.3905-1G>A
XM_017011107.2:c.3884-1G>A XP_016866596.1:n.3884-1G>A
XR_002956289.1:n.4276-1G>A