Canonical Allele Identifier: CA1468189733
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs1720146201
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73455920A>T , CM000666.2:g.73455920A>T GRCh38
NC_000004.11:g.74321637A>T , CM000666.1:g.74321637A>T GRCh37
NC_000004.10:g.74540501A>T NCBI36
NG_023028.1:g.24705A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.*300A>T MANE Select ENSP00000379138.2:n.*300A>T
ENST00000395792.6:c.*300A>T ENSP00000379138.2:n.*300A>T
NM_001134.3:c.*300A>T MANE Select NP_001125.1:n.*300A>T
NM_001354717.2:c.*300A>T NP_001341646.2:n.*300A>T
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