Canonical Allele Identifier: CA2325096969

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1599346412

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879472T>C , CM000681.2:g.15879472T>C	GRCh38
NC_000019.9:g.15990282T>C , CM000681.1:g.15990282T>C	GRCh37
NC_000019.8:g.15851282T>C	NCBI36
NG_007971.2:g.23603A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.1315-44A>G MANE Select	ENSP00000221700.3:n.1315-44A>G
ENST00000011989.11:c.1315-44A>G	ENSP00000011989.8:n.1315-44A>G
ENST00000221700.10:c.1315-44A>G	ENSP00000221700.3:n.1315-44A>G
ENST00000392846.7:n.1258-44A>G
ENST00000589654.2:c.103-44A>G
NM_001082.4:c.1315-44A>G	NP_001073.3:n.1315-44A>G
NM_001082.5:c.1315-44A>G MANE Select	NP_001073.3:n.1315-44A>G