Canonical Allele Identifier: CA2670971471
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73456001-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73456001T>A , CM000666.2:g.73456001T>A GRCh38
NC_000004.11:g.74321718T>A , CM000666.1:g.74321718T>A GRCh37
NC_000004.10:g.74540582T>A NCBI36
NG_023028.1:g.24786T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*381T>A MANE Select ENSP00000379138.2:n.*381T>A
ENST00000395792.6:c.*381T>A ENSP00000379138.2:n.*381T>A
NM_001134.3:c.*381T>A MANE Select NP_001125.1:n.*381T>A
NM_001354717.2:c.*381T>A NP_001341646.2:n.*381T>A
Search 100 bp 5'
Search 100 bp 3'