Canonical Allele Identifier: CA414510026
Gene: AFF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.148662530A>G , CM000685.2:g.148662530A>G GRCh38
NC_000023.10:g.147744051A>G , CM000685.1:g.147744051A>G GRCh37
NC_000023.9:g.147551743A>G NCBI36
NG_016313.1:g.166913A>G
NG_016313.2:g.166912A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370460.7:c.803A>G MANE Select ENSP00000359489.2:p.Gln268Arg
ENST00000342251.7:c.791A>G ENSP00000345459.4:p.Gln264Arg
ENST00000370457.9:c.803A>G ENSP00000359486.6:p.Gln268Arg
ENST00000370458.5:c.791A>G ENSP00000359487.1:p.Gln264Arg
ENST00000370460.6:c.803A>G ENSP00000359489.2:p.Gln268Arg
NM_001169122.1:c.791A>G NP_001162593.1:p.Gln264Arg
NM_001169123.1:c.791A>G NP_001162594.1:p.Gln264Arg
NM_001169124.1:c.803A>G NP_001162595.1:p.Gln268Arg
NM_001169125.1:c.791A>G NP_001162596.1:p.Gln264Arg
NM_002025.3:c.803A>G NP_002016.2:p.Gln268Arg
NM_001169122.2:c.791A>G NP_001162593.1:p.Gln264Arg
NM_001169123.2:c.791A>G NP_001162594.1:p.Gln264Arg
NM_001169124.2:c.803A>G NP_001162595.1:p.Gln268Arg
NM_001169125.2:c.791A>G NP_001162596.1:p.Gln264Arg
NM_002025.4:c.803A>G MANE Select NP_002016.2:p.Gln268Arg