Canonical Allele Identifier: CA1064126995
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs1720146040
gnomAD v3: 4-73455906-A-C
gnomAD v4: 4-73455906-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455906A>C , CM000666.2:g.73455906A>C GRCh38
NC_000004.11:g.74321623A>C , CM000666.1:g.74321623A>C GRCh37
NC_000004.10:g.74540487A>C NCBI36
NG_023028.1:g.24691A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*286A>C MANE Select ENSP00000379138.2:n.*286A>C
ENST00000395792.6:c.*286A>C ENSP00000379138.2:n.*286A>C
NM_001134.3:c.*286A>C MANE Select NP_001125.1:n.*286A>C
NM_001354717.2:c.*286A>C NP_001341646.2:n.*286A>C
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