Canonical Allele Identifier: CA2325105562
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897498G= , CM000681.2:g.15897498G= GRCh38
NC_000019.9:g.16008308G= , CM000681.1:g.16008308G= GRCh37
NC_000019.8:g.15869308G= NCBI36
NG_007971.2:g.5577C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.114C= MANE Select ENSP00000221700.3:p.Thr38=
ENST00000011989.11:c.114C= ENSP00000011989.8:p.Thr38=
ENST00000221700.10:c.114C= ENSP00000221700.3:p.Thr38=
ENST00000392846.7:n.49+528C=
ENST00000586927.2:c.114C= ENSP00000465514.1:p.Thr38=
ENST00000587671.2:c.114C= ENSP00000467443.2:p.Thr38=
ENST00000608168.1:n.167C=
NM_001082.4:c.114C= NP_001073.3:p.Thr38=
NM_001082.5:c.114C= MANE Select NP_001073.3:p.Thr38=