Canonical Allele Identifier: CA2670971423
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73455908-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455908G>T , CM000666.2:g.73455908G>T GRCh38
NC_000004.11:g.74321625G>T , CM000666.1:g.74321625G>T GRCh37
NC_000004.10:g.74540489G>T NCBI36
NG_023028.1:g.24693G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*288G>T MANE Select ENSP00000379138.2:n.*288G>T
ENST00000395792.6:c.*288G>T ENSP00000379138.2:n.*288G>T
NM_001134.3:c.*288G>T MANE Select NP_001125.1:n.*288G>T
NM_001354717.2:c.*288G>T NP_001341646.2:n.*288G>T
Search 100 bp 5'
Search 100 bp 3'