Canonical Allele Identifier: CA2325105689
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897707C= , CM000681.2:g.15897707C= GRCh38
NC_000019.9:g.16008517C= , CM000681.1:g.16008517C= GRCh37
NC_000019.8:g.15869517C= NCBI36
NG_007971.2:g.5368G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-95G= MANE Select ENSP00000221700.3:n.-1-95G=
ENST00000011989.11:c.-1-95G= ENSP00000011989.8:n.-1-95G=
ENST00000221700.10:c.-1-95G= ENSP00000221700.3:n.-1-95G=
ENST00000392846.7:n.49+319G=
ENST00000586927.2:c.-96G= ENSP00000465514.1:n.-96G=
ENST00000587671.2:c.-1-95G= ENSP00000467443.2:n.-1-95G=
ENST00000608168.1:n.53-95G=
NM_001082.4:c.-1-95G= NP_001073.3:n.-1-95G=
NM_001082.5:c.-1-95G= MANE Select NP_001073.3:n.-1-95G=
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