Canonical Allele Identifier: CA2325096789
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879130A= , CM000681.2:g.15879130A= GRCh38
NC_000019.9:g.15989940A= , CM000681.1:g.15989940A= GRCh37
NC_000019.8:g.15850940A= NCBI36
NG_007971.2:g.23945T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1398-194T= MANE Select ENSP00000221700.3:n.1398-194T=
ENST00000011989.11:c.1398-194T= ENSP00000011989.8:n.1398-194T=
ENST00000221700.10:c.1398-194T= ENSP00000221700.3:n.1398-194T=
ENST00000392846.7:n.1341-194T=
ENST00000589654.2:c.186-194T=
NM_001082.4:c.1398-194T= NP_001073.3:n.1398-194T=
NM_001082.5:c.1398-194T= MANE Select NP_001073.3:n.1398-194T=
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