Canonical Allele Identifier: CA2325105522
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897410T= , CM000681.2:g.15897410T= GRCh38
NC_000019.9:g.16008220T= , CM000681.1:g.16008220T= GRCh37
NC_000019.8:g.15869220T= NCBI36
NG_007971.2:g.5665A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.198+4A= MANE Select ENSP00000221700.3:n.198+4A=
ENST00000011989.11:c.198+4A= ENSP00000011989.8:n.198+4A=
ENST00000221700.10:c.198+4A= ENSP00000221700.3:n.198+4A=
ENST00000392846.7:n.49+616A=
ENST00000586927.2:c.198+4A= ENSP00000465514.1:n.198+4A=
ENST00000587671.2:c.198+4A= ENSP00000467443.2:n.198+4A=
ENST00000608168.1:n.251+4A=
NM_001082.4:c.198+4A= NP_001073.3:n.198+4A=
NM_001082.5:c.198+4A= MANE Select NP_001073.3:n.198+4A=
Search 100 bp 5'
Search 100 bp 3'