Canonical Allele Identifier: CA404580057

Gene: CYP4F2

Linked Data

• MyVariant Identifiers: chr19:g.16008407G>T (hg19) ; chr19:g.15897597G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897597G>T , CM000681.2:g.15897597G>T	GRCh38
NC_000019.9:g.16008407G>T , CM000681.1:g.16008407G>T	GRCh37
NC_000019.8:g.15869407G>T	NCBI36
NG_007971.2:g.5478C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.15C>A MANE Select	ENSP00000221700.3:p.Ser5Arg
ENST00000011989.11:c.15C>A	ENSP00000011989.8:p.Ser5Arg
ENST00000221700.10:c.15C>A	ENSP00000221700.3:p.Ser5Arg
ENST00000392846.7:n.49+429C>A
ENST00000586927.2:c.15C>A	ENSP00000465514.1:p.Ser5Arg
ENST00000587671.2:c.15C>A	ENSP00000467443.2:p.Ser5Arg
ENST00000608168.1:n.68C>A
NM_001082.4:c.15C>A	NP_001073.3:p.Ser5Arg
NM_001082.5:c.15C>A MANE Select	NP_001073.3:p.Ser5Arg