Canonical Allele Identifier: CA2670971424
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73455909-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455909G>C , CM000666.2:g.73455909G>C GRCh38
NC_000004.11:g.74321626G>C , CM000666.1:g.74321626G>C GRCh37
NC_000004.10:g.74540490G>C NCBI36
NG_023028.1:g.24694G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*289G>C MANE Select ENSP00000379138.2:n.*289G>C
ENST00000395792.6:c.*289G>C ENSP00000379138.2:n.*289G>C
NM_001134.3:c.*289G>C MANE Select NP_001125.1:n.*289G>C
NM_001354717.2:c.*289G>C NP_001341646.2:n.*289G>C
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