Canonical Allele Identifier: CA414512266
Community Standard Title: NM_002025.4(AFF2):c.3163A>G (p.Ser1055Gly)
Gene: AFF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.148967039A>G , CM000685.2:g.148967039A>G GRCh38
NC_000023.10:g.148048569A>G , CM000685.1:g.148048569A>G GRCh37
NC_000023.9:g.147856263A>G NCBI36
NG_016313.1:g.471431A>G
NG_016313.2:g.471421A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002025.4:c.3163A>G MANE Select NP_002016.2:p.Ser1055Gly
ENST00000370460.7:c.3163A>G MANE Select ENSP00000359489.2:p.Ser1055Gly
NM_001169122.1:c.3058A>G NP_001162593.1:p.Ser1020Gly
NM_001169122.2:c.3058A>G NP_001162593.1:p.Ser1020Gly
NM_001169123.1:c.3133A>G NP_001162594.1:p.Ser1045Gly
NM_001169123.2:c.3133A>G NP_001162594.1:p.Ser1045Gly
NM_001169124.1:c.3058A>G NP_001162595.1:p.Ser1020Gly
NM_001169124.2:c.3058A>G NP_001162595.1:p.Ser1020Gly
NM_001169125.1:c.3046A>G NP_001162596.1:p.Ser1016Gly
NM_001169125.2:c.3046A>G NP_001162596.1:p.Ser1016Gly
NM_001170628.1:c.2086A>G NP_001164099.1:p.Ser696Gly
NM_002025.3:c.3163A>G NP_002016.2:p.Ser1055Gly
ENST00000286437.7:c.2086A>G ENSP00000286437.5:p.Ser696Gly
ENST00000342251.7:c.3058A>G ENSP00000345459.4:p.Ser1020Gly
ENST00000370457.9:c.3058A>G ENSP00000359486.6:p.Ser1020Gly
ENST00000370460.6:c.3163A>G ENSP00000359489.2:p.Ser1055Gly
ENST00000671877.1:n.2176A>G