Canonical Allele Identifier: CA798278070
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs1166711915
gnomAD v3: 4-73455891-A-G
gnomAD v4: 4-73455891-A-G
MyVariant Identifiers: chr4:g.74321608A>G (hg19) chr4:g.73455891A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455891A>G , CM000666.2:g.73455891A>G GRCh38
NC_000004.11:g.74321608A>G , CM000666.1:g.74321608A>G GRCh37
NC_000004.10:g.74540472A>G NCBI36
NG_023028.1:g.24676A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*271A>G MANE Select ENSP00000379138.2:n.*271A>G
ENST00000395792.6:c.*271A>G ENSP00000379138.2:n.*271A>G
NM_001134.3:c.*271A>G MANE Select NP_001125.1:n.*271A>G
NM_001354717.2:c.*271A>G NP_001341646.2:n.*271A>G
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