Canonical Allele Identifier: CA2813750326

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879128A>G , CM000681.2:g.15879128A>G	GRCh38
NC_000019.9:g.15989938A>G , CM000681.1:g.15989938A>G	GRCh37
NC_000019.8:g.15850938A>G	NCBI36
NG_007971.2:g.23947T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1398-192T>C MANE Select	ENSP00000221700.3:n.1398-192T>C
ENST00000011989.11:c.1398-192T>C	ENSP00000011989.8:n.1398-192T>C
ENST00000221700.10:c.1398-192T>C	ENSP00000221700.3:n.1398-192T>C
ENST00000392846.7:n.1341-192T>C
ENST00000589654.2:c.186-192T>C
NM_001082.4:c.1398-192T>C	NP_001073.3:n.1398-192T>C
NM_001082.5:c.1398-192T>C MANE Select	NP_001073.3:n.1398-192T>C