Canonical Allele Identifier: CA2325105526
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897417G= , CM000681.2:g.15897417G= GRCh38
NC_000019.9:g.16008227G= , CM000681.1:g.16008227G= GRCh37
NC_000019.8:g.15869227G= NCBI36
NG_007971.2:g.5658C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.195C= MANE Select ENSP00000221700.3:p.Gly65=
ENST00000011989.11:c.195C= ENSP00000011989.8:p.Gly65=
ENST00000221700.10:c.195C= ENSP00000221700.3:p.Gly65=
ENST00000392846.7:n.49+609C=
ENST00000586927.2:c.195C= ENSP00000465514.1:p.Gly65=
ENST00000587671.2:c.195C= ENSP00000467443.2:p.Gly65=
ENST00000608168.1:n.248C=
NM_001082.4:c.195C= NP_001073.3:p.Gly65=
NM_001082.5:c.195C= MANE Select NP_001073.3:p.Gly65=