Canonical Allele Identifier: CA505872662

Gene: CYP4F2

Linked Data

• MyVariant Identifiers: chr19:g.16008410C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897600C>T , CM000681.2:g.15897600C>T	GRCh38
NC_000019.9:g.16008410C>T , CM000681.1:g.16008410C>T	GRCh37
NC_000019.8:g.15869410C>T	NCBI36
NG_007971.2:g.5475G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.12G>A MANE Select	ENSP00000221700.3:p.Leu4=
ENST00000011989.11:c.12G>A	ENSP00000011989.8:p.Leu4=
ENST00000221700.10:c.12G>A	ENSP00000221700.3:p.Leu4=
ENST00000392846.7:n.49+426G>A
ENST00000586927.2:c.12G>A	ENSP00000465514.1:p.Leu4=
ENST00000587671.2:c.12G>A	ENSP00000467443.2:p.Leu4=
ENST00000608168.1:n.65G>A
NM_001082.4:c.12G>A	NP_001073.3:p.Leu4=
NM_001082.5:c.12G>A MANE Select	NP_001073.3:p.Leu4=