Canonical Allele Identifier: CA1468189695
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs1720144240
gnomAD v4: 4-73455832-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455832G>A , CM000666.2:g.73455832G>A GRCh38
NC_000004.11:g.74321549G>A , CM000666.1:g.74321549G>A GRCh37
NC_000004.10:g.74540413G>A NCBI36
NG_023028.1:g.24617G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*212G>A MANE Select ENSP00000379138.2:n.*212G>A
ENST00000395792.6:c.*212G>A ENSP00000379138.2:n.*212G>A
NM_001134.3:c.*212G>A MANE Select NP_001125.1:n.*212G>A
NM_001354717.2:c.*212G>A NP_001341646.2:n.*212G>A
Search 100 bp 5'
Search 100 bp 3'