Canonical Allele Identifier: CA2325105735
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897784C= , CM000681.2:g.15897784C= GRCh38
NC_000019.9:g.16008594C= , CM000681.1:g.16008594C= GRCh37
NC_000019.8:g.15869594C= NCBI36
NG_007971.2:g.5291G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-172G= MANE Select ENSP00000221700.3:n.-1-172G=
ENST00000011989.11:c.-1-172G= ENSP00000011989.8:n.-1-172G=
ENST00000221700.10:c.-1-172G= ENSP00000221700.3:n.-1-172G=
ENST00000392846.7:n.49+242G=
ENST00000587671.2:c.-1-172G= ENSP00000467443.2:n.-1-172G=
ENST00000608168.1:n.53-172G=
NM_001082.4:c.-1-172G= NP_001073.3:n.-1-172G=
NM_001082.5:c.-1-172G= MANE Select NP_001073.3:n.-1-172G=