Canonical Allele Identifier: CA1468189775
Gene: AFP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455976C= , CM000666.2:g.73455976C= GRCh38
NC_000004.11:g.74321693C= , CM000666.1:g.74321693C= GRCh37
NC_000004.10:g.74540557C= NCBI36
NG_023028.1:g.24761C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*356C= MANE Select ENSP00000379138.2:n.*356C=
ENST00000395792.6:c.*356C= ENSP00000379138.2:n.*356C=
NM_001134.3:c.*356C= MANE Select NP_001125.1:n.*356C=
NM_001354717.2:c.*356C= NP_001341646.2:n.*356C=
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