Canonical Allele Identifier: CA2325096996
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879532C= , CM000681.2:g.15879532C= GRCh38
NC_000019.9:g.15990342C= , CM000681.1:g.15990342C= GRCh37
NC_000019.8:g.15851342C= NCBI36
NG_007971.2:g.23543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1314+72G= MANE Select ENSP00000221700.3:n.1314+72G=
ENST00000011989.11:c.1314+72G= ENSP00000011989.8:n.1314+72G=
ENST00000221700.10:c.1314+72G= ENSP00000221700.3:n.1314+72G=
ENST00000392846.7:n.1257+72G=
ENST00000589654.2:c.103-104G=
NM_001082.4:c.1314+72G= NP_001073.3:n.1314+72G=
NM_001082.5:c.1314+72G= MANE Select NP_001073.3:n.1314+72G=