Canonical Allele Identifier: CA2670971411
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73455894-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455894T>G , CM000666.2:g.73455894T>G GRCh38
NC_000004.11:g.74321611T>G , CM000666.1:g.74321611T>G GRCh37
NC_000004.10:g.74540475T>G NCBI36
NG_023028.1:g.24679T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*274T>G MANE Select ENSP00000379138.2:n.*274T>G
ENST00000395792.6:c.*274T>G ENSP00000379138.2:n.*274T>G
NM_001134.3:c.*274T>G MANE Select NP_001125.1:n.*274T>G
NM_001354717.2:c.*274T>G NP_001341646.2:n.*274T>G
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