Canonical Allele Identifier: CA10536825
Gene: AFF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.148662293C>T , CM000685.2:g.148662293C>T GRCh38
NC_000023.10:g.147743814C>T , CM000685.1:g.147743814C>T GRCh37
NC_000023.9:g.147551506C>T NCBI36
NG_016313.1:g.166676C>T
NG_016313.2:g.166675C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370460.7:c.566C>T MANE Select ENSP00000359489.2:p.Ser189Phe
ENST00000342251.7:c.554C>T ENSP00000345459.4:p.Ser185Phe
ENST00000370457.9:c.566C>T ENSP00000359486.6:p.Ser189Phe
ENST00000370458.5:c.554C>T ENSP00000359487.1:p.Ser185Phe
ENST00000370460.6:c.566C>T ENSP00000359489.2:p.Ser189Phe
NM_001169122.1:c.554C>T NP_001162593.1:p.Ser185Phe
NM_001169123.1:c.554C>T NP_001162594.1:p.Ser185Phe
NM_001169124.1:c.566C>T NP_001162595.1:p.Ser189Phe
NM_001169125.1:c.554C>T NP_001162596.1:p.Ser185Phe
NM_002025.3:c.566C>T NP_002016.2:p.Ser189Phe
NM_001169122.2:c.554C>T NP_001162593.1:p.Ser185Phe
NM_001169123.2:c.554C>T NP_001162594.1:p.Ser185Phe
NM_001169124.2:c.566C>T NP_001162595.1:p.Ser189Phe
NM_001169125.2:c.554C>T NP_001162596.1:p.Ser185Phe
NM_002025.4:c.566C>T MANE Select NP_002016.2:p.Ser189Phe