Canonical Allele Identifier: CA2325105692
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897711G= , CM000681.2:g.15897711G= GRCh38
NC_000019.9:g.16008521G= , CM000681.1:g.16008521G= GRCh37
NC_000019.8:g.15869521G= NCBI36
NG_007971.2:g.5364C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-99C= MANE Select ENSP00000221700.3:n.-1-99C=
ENST00000011989.11:c.-1-99C= ENSP00000011989.8:n.-1-99C=
ENST00000221700.10:c.-1-99C= ENSP00000221700.3:n.-1-99C=
ENST00000392846.7:n.49+315C=
ENST00000586927.2:c.-100C= ENSP00000465514.1:n.-100C=
ENST00000587671.2:c.-1-99C= ENSP00000467443.2:n.-1-99C=
ENST00000608168.1:n.53-99C=
NM_001082.4:c.-1-99C= NP_001073.3:n.-1-99C=
NM_001082.5:c.-1-99C= MANE Select NP_001073.3:n.-1-99C=
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