Canonical Allele Identifier: CA10536810
Gene: AFF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.148662208C>A , CM000685.2:g.148662208C>A GRCh38
NC_000023.10:g.147743729C>A , CM000685.1:g.147743729C>A GRCh37
NC_000023.9:g.147551421C>A NCBI36
NG_016313.1:g.166591C>A
NG_016313.2:g.166590C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370460.7:c.481C>A MANE Select ENSP00000359489.2:p.Arg161Ser
ENST00000342251.7:c.469C>A ENSP00000345459.4:p.Arg157Ser
ENST00000370457.9:c.481C>A ENSP00000359486.6:p.Arg161Ser
ENST00000370458.5:c.469C>A ENSP00000359487.1:p.Arg157Ser
ENST00000370460.6:c.481C>A ENSP00000359489.2:p.Arg161Ser
NM_001169122.1:c.469C>A NP_001162593.1:p.Arg157Ser
NM_001169123.1:c.469C>A NP_001162594.1:p.Arg157Ser
NM_001169124.1:c.481C>A NP_001162595.1:p.Arg161Ser
NM_001169125.1:c.469C>A NP_001162596.1:p.Arg157Ser
NM_002025.3:c.481C>A NP_002016.2:p.Arg161Ser
NM_001169122.2:c.469C>A NP_001162593.1:p.Arg157Ser
NM_001169123.2:c.469C>A NP_001162594.1:p.Arg157Ser
NM_001169124.2:c.481C>A NP_001162595.1:p.Arg161Ser
NM_001169125.2:c.469C>A NP_001162596.1:p.Arg157Ser
NM_002025.4:c.481C>A MANE Select NP_002016.2:p.Arg161Ser