Canonical Allele Identifier: CA2325101761
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889283T= , CM000681.2:g.15889283T= GRCh38
NC_000019.9:g.16000093T= , CM000681.1:g.16000093T= GRCh37
NC_000019.8:g.15861093T= NCBI36
NG_007971.2:g.13792A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.918+140A= MANE Select ENSP00000221700.3:n.918+140A=
ENST00000011989.11:c.918+140A= ENSP00000011989.8:n.918+140A=
ENST00000221700.10:c.918+140A= ENSP00000221700.3:n.918+140A=
ENST00000392846.7:n.861+140A=
ENST00000587671.2:c.*503+140A= ENSP00000467443.2:n.*503+140A=
NM_001082.4:c.918+140A= NP_001073.3:n.918+140A=
NM_001082.5:c.918+140A= MANE Select NP_001073.3:n.918+140A=
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