Canonical Allele Identifier: CA2325105657
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897656G= , CM000681.2:g.15897656G= GRCh38
NC_000019.9:g.16008466G= , CM000681.1:g.16008466G= GRCh37
NC_000019.8:g.15869466G= NCBI36
NG_007971.2:g.5419C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-44C= MANE Select ENSP00000221700.3:n.-1-44C=
ENST00000011989.11:c.-1-44C= ENSP00000011989.8:n.-1-44C=
ENST00000221700.10:c.-1-44C= ENSP00000221700.3:n.-1-44C=
ENST00000392846.7:n.49+370C=
ENST00000586927.2:c.-45C= ENSP00000465514.1:n.-45C=
ENST00000587671.2:c.-1-44C= ENSP00000467443.2:n.-1-44C=
ENST00000608168.1:n.53-44C=
NM_001082.4:c.-1-44C= NP_001073.3:n.-1-44C=
NM_001082.5:c.-1-44C= MANE Select NP_001073.3:n.-1-44C=