Canonical Allele Identifier: CA2325105715
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897747G= , CM000681.2:g.15897747G= GRCh38
NC_000019.9:g.16008557G= , CM000681.1:g.16008557G= GRCh37
NC_000019.8:g.15869557G= NCBI36
NG_007971.2:g.5328C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-135C= MANE Select ENSP00000221700.3:n.-1-135C=
ENST00000011989.11:c.-1-135C= ENSP00000011989.8:n.-1-135C=
ENST00000221700.10:c.-1-135C= ENSP00000221700.3:n.-1-135C=
ENST00000392846.7:n.49+279C=
ENST00000587671.2:c.-1-135C= ENSP00000467443.2:n.-1-135C=
ENST00000608168.1:n.53-135C=
NM_001082.4:c.-1-135C= NP_001073.3:n.-1-135C=
NM_001082.5:c.-1-135C= MANE Select NP_001073.3:n.-1-135C=