Canonical Allele Identifier: CA2706482524
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs2149337816
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455876G>A , CM000666.2:g.73455876G>A GRCh38
NC_000004.11:g.74321593G>A , CM000666.1:g.74321593G>A GRCh37
NC_000004.10:g.74540457G>A NCBI36
NG_023028.1:g.24661G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*256G>A MANE Select ENSP00000379138.2:n.*256G>A
ENST00000395792.6:c.*256G>A ENSP00000379138.2:n.*256G>A
NM_001134.3:c.*256G>A MANE Select NP_001125.1:n.*256G>A
NM_001354717.2:c.*256G>A NP_001341646.2:n.*256G>A
Search 100 bp 5'
Search 100 bp 3'