Canonical Allele Identifier: CA1468189726
Gene: AFP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455898A= , CM000666.2:g.73455898A= GRCh38
NC_000004.11:g.74321615A= , CM000666.1:g.74321615A= GRCh37
NC_000004.10:g.74540479A= NCBI36
NG_023028.1:g.24683A=

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*278A= MANE Select ENSP00000379138.2:n.*278A=
ENST00000395792.6:c.*278A= ENSP00000379138.2:n.*278A=
NM_001134.3:c.*278A= MANE Select NP_001125.1:n.*278A=
NM_001354717.2:c.*278A= NP_001341646.2:n.*278A=
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