Canonical Allele Identifier: CA2576658998
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879466T>A , CM000681.2:g.15879466T>A GRCh38
NC_000019.9:g.15990276T>A , CM000681.1:g.15990276T>A GRCh37
NC_000019.8:g.15851276T>A NCBI36
NG_007971.2:g.23609A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.1315-38A>T MANE Select ENSP00000221700.3:n.1315-38A>T
ENST00000011989.11:c.1315-38A>T ENSP00000011989.8:n.1315-38A>T
ENST00000221700.10:c.1315-38A>T ENSP00000221700.3:n.1315-38A>T
ENST00000392846.7:n.1258-38A>T
ENST00000589654.2:c.103-38A>T
NM_001082.4:c.1315-38A>T NP_001073.3:n.1315-38A>T
NM_001082.5:c.1315-38A>T MANE Select NP_001073.3:n.1315-38A>T
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