Canonical Allele Identifier: CA439800134

Gene: AFP

Linked Data

• gnomAD v4: 4-73442317-A-G
• MyVariant Identifiers: chr4:g.74308034A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442317A>G , CM000666.2:g.73442317A>G	GRCh38
NC_000004.11:g.74308034A>G , CM000666.1:g.74308034A>G	GRCh37
NC_000004.10:g.74526898A>G	NCBI36
NG_023028.1:g.11102A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.504A>G MANE Select	ENSP00000379138.2:p.Arg168=
ENST00000226359.2:c.504A>G	ENSP00000226359.2:p.Arg168=
ENST00000395792.6:c.504A>G	ENSP00000379138.2:p.Arg168=
NM_001134.2:c.504A>G	NP_001125.1:p.Arg168=
XM_011531704.1:c.501A>G	XP_011530006.1:p.Arg167=
NM_001354717.1:c.30A>G	NP_001341646.1:p.Arg10=
NM_001134.3:c.504A>G MANE Select	NP_001125.1:p.Arg168=
NM_001354717.2:c.30A>G	NP_001341646.2:p.Arg10=