Canonical Allele Identifier: CA2762178733

Gene: AFP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73455810T>C , CM000666.2:g.73455810T>C	GRCh38
NC_000004.11:g.74321527T>C , CM000666.1:g.74321527T>C	GRCh37
NC_000004.10:g.74540391T>C	NCBI36
NG_023028.1:g.24595T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.*190T>C MANE Select	ENSP00000379138.2:n.*190T>C
ENST00000395792.6:c.*190T>C	ENSP00000379138.2:n.*190T>C
NM_001134.3:c.*190T>C MANE Select	NP_001125.1:n.*190T>C
NM_001354717.2:c.*190T>C	NP_001341646.2:n.*190T>C