Canonical Allele Identifier: CA1468189723
Gene: AFP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455892G= , CM000666.2:g.73455892G= GRCh38
NC_000004.11:g.74321609G= , CM000666.1:g.74321609G= GRCh37
NC_000004.10:g.74540473G= NCBI36
NG_023028.1:g.24677G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*272G= MANE Select ENSP00000379138.2:n.*272G=
ENST00000395792.6:c.*272G= ENSP00000379138.2:n.*272G=
NM_001134.3:c.*272G= MANE Select NP_001125.1:n.*272G=
NM_001354717.2:c.*272G= NP_001341646.2:n.*272G=
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