Canonical Allele Identifier: CA2670971422
Gene: AFP HGNC NCBI

Linked Data

gnomAD v4: 4-73455908-G-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*288G>C MANE Select ENSP00000379138.2:n.*288G>C
ENST00000395792.6:c.*288G>C ENSP00000379138.2:n.*288G>C
NM_001134.3:c.*288G>C MANE Select NP_001125.1:n.*288G>C
NM_001354717.2:c.*288G>C NP_001341646.2:n.*288G>C
Search 100 bp 5'
Search 100 bp 3'