Canonical Allele Identifier: CA1468189679
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs1720143465

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455785C>G , CM000666.2:g.73455785C>G GRCh38
NC_000004.11:g.74321502C>G , CM000666.1:g.74321502C>G GRCh37
NC_000004.10:g.74540366C>G NCBI36
NG_023028.1:g.24570C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395792.7:c.*165C>G MANE Select ENSP00000379138.2:n.*165C>G
ENST00000395792.6:c.*165C>G ENSP00000379138.2:n.*165C>G
NM_001134.2:c.*165C>G NP_001125.1:n.*165C>G
NM_001354717.1:c.*165C>G NP_001341646.1:n.*165C>G
NM_001134.3:c.*165C>G MANE Select NP_001125.1:n.*165C>G
NM_001354717.2:c.*165C>G NP_001341646.2:n.*165C>G