Canonical Allele Identifier: CA2325096836
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879219T= , CM000681.2:g.15879219T= GRCh38
NC_000019.9:g.15990029T= , CM000681.1:g.15990029T= GRCh37
NC_000019.8:g.15851029T= NCBI36
NG_007971.2:g.23856A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+127A= MANE Select ENSP00000221700.3:n.1397+127A=
ENST00000011989.11:c.1397+127A= ENSP00000011989.8:n.1397+127A=
ENST00000221700.10:c.1397+127A= ENSP00000221700.3:n.1397+127A=
ENST00000392846.7:n.1340+127A=
ENST00000589654.2:c.185+127A=
NM_001082.4:c.1397+127A= NP_001073.3:n.1397+127A=
NM_001082.5:c.1397+127A= MANE Select NP_001073.3:n.1397+127A=
Search 100 bp 5'
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