Canonical Allele Identifier: CA2534519054
Gene: AFP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455834A>G , CM000666.2:g.73455834A>G GRCh38
NC_000004.11:g.74321551A>G , CM000666.1:g.74321551A>G GRCh37
NC_000004.10:g.74540415A>G NCBI36
NG_023028.1:g.24619A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*214A>G MANE Select ENSP00000379138.2:n.*214A>G
ENST00000395792.6:c.*214A>G ENSP00000379138.2:n.*214A>G
NM_001134.3:c.*214A>G MANE Select NP_001125.1:n.*214A>G
NM_001354717.2:c.*214A>G NP_001341646.2:n.*214A>G