Canonical Allele Identifier: CA2325096908

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879338G= , CM000681.2:g.15879338G=	GRCh38
NC_000019.9:g.15990148G= , CM000681.1:g.15990148G=	GRCh37
NC_000019.8:g.15851148G=	NCBI36
NG_007971.2:g.23737C=

Transcript Alleles

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