Canonical Allele Identifier: CA439800173
Gene: AFP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.74308070T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73442353T>A , CM000666.2:g.73442353T>A GRCh38
NC_000004.11:g.74308070T>A , CM000666.1:g.74308070T>A GRCh37
NC_000004.10:g.74526934T>A NCBI36
NG_023028.1:g.11138T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.540T>A MANE Select ENSP00000379138.2:p.Leu180=
ENST00000226359.2:c.540T>A ENSP00000226359.2:p.Leu180=
ENST00000395792.6:c.540T>A ENSP00000379138.2:p.Leu180=
NM_001134.2:c.540T>A NP_001125.1:p.Leu180=
XM_011531704.1:c.537T>A XP_011530006.1:p.Leu179=
NM_001354717.1:c.66T>A NP_001341646.1:p.Leu22=
NM_001134.3:c.540T>A MANE Select NP_001125.1:p.Leu180=
NM_001354717.2:c.66T>A NP_001341646.2:p.Leu22=
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