Canonical Allele Identifier: CA2670971367
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73455784-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455784T>C , CM000666.2:g.73455784T>C GRCh38
NC_000004.11:g.74321501T>C , CM000666.1:g.74321501T>C GRCh37
NC_000004.10:g.74540365T>C NCBI36
NG_023028.1:g.24569T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*164T>C MANE Select ENSP00000379138.2:n.*164T>C
ENST00000395792.6:c.*164T>C ENSP00000379138.2:n.*164T>C
NM_001134.2:c.*164T>C NP_001125.1:n.*164T>C
XM_011531704.1:c.*164T>C XP_011530006.1:n.*164T>C
NM_001354717.1:c.*164T>C NP_001341646.1:n.*164T>C
NM_001134.3:c.*164T>C MANE Select NP_001125.1:n.*164T>C
NM_001354717.2:c.*164T>C NP_001341646.2:n.*164T>C
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