Canonical Allele Identifier: CA1675367800
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156829358T= , CM000668.2:g.156829358T= GRCh38
NC_000006.11:g.157150492T= , CM000668.1:g.157150492T= GRCh37
NC_000006.10:g.157192184T= NCBI36
NG_032093.1:g.56429T=
NG_032093.2:g.56429T=
NG_066624.1:g.58333T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.1923T= ENSP00000055163.8:p.Tyr641=
ENST00000414678.8:c.1923T= ENSP00000412835.3:p.Tyr641=
ENST00000637015.2:c.1923T= ENSP00000489729.2:p.Tyr641=
ENST00000346085.10:c.1923T= ENSP00000344546.5:p.Tyr641=
ENST00000350026.10:c.1674T= ENSP00000055163.7:p.Tyr558=
ENST00000414678.7:c.171T= ENSP00000412835.2:p.Tyr57=
ENST00000494260.2:c.204T= ENSP00000490094.1:p.Tyr68=
ENST00000636607.1:c.186T= ENSP00000490050.1:p.Tyr62=
ENST00000636748.1:c.204T= ENSP00000489917.1:p.Tyr68=
ENST00000636930.2:c.1923T= MANE Select ENSP00000490491.2:p.Tyr641=
ENST00000637910.1:n.204T=
ENST00000638000.1:c.140T=
ENST00000647938.1:c.1674T= ENSP00000498155.1:p.Tyr558=
ENST00000674190.1:n.630T=
ENST00000674298.1:c.1663T=
ENST00000346085.9:c.1674T= ENSP00000344546.4:p.Tyr558=
ENST00000350026.9:c.1674T= ENSP00000055163.7:p.Tyr558=
ENST00000414678.6:c.171T= ENSP00000412835.2:p.Tyr57=
ENST00000494260.1:n.132T=
NM_017519.2:c.1674T= NP_059989.2:p.Tyr558=
NM_020732.3:c.1674T= NP_065783.3:p.Tyr558=
XM_005267069.3:c.1674T= XP_005267126.2:p.Tyr558=
XM_011535984.1:c.543T= XP_011534286.1:p.Tyr181=
XM_011535985.1:c.543T= XP_011534287.1:p.Tyr181=
XM_011535986.1:c.123T= XP_011534288.1:p.Tyr41=
NM_001346813.1:c.1674T= NP_001333742.1:p.Tyr558=
XM_011535984.2:c.1674T= XP_011534286.2:p.Tyr558=
XM_017011103.2:c.1674T= XP_016866592.1:p.Tyr558=
XM_017011104.1:c.1674T= XP_016866593.1:p.Tyr558=
XM_017011105.2:c.1674T= XP_016866594.1:p.Tyr558=
XM_017011106.2:c.1674T= XP_016866595.1:p.Tyr558=
XM_017011107.2:c.1674T= XP_016866596.1:p.Tyr558=
XR_002956289.1:n.1757T=
NM_001371656.1:c.1923T= NP_001358585.1:p.Tyr641=
NM_001374820.1:c.1923T= NP_001361749.1:p.Tyr641=
NM_001374828.1:c.1923T= MANE Select NP_001361757.1:p.Tyr641=
NM_017519.3:c.1923T= NP_059989.3:p.Tyr641=