Canonical Allele Identifier: CA505872615
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16008353C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897543C>A , CM000681.2:g.15897543C>A GRCh38
NC_000019.9:g.16008353C>A , CM000681.1:g.16008353C>A GRCh37
NC_000019.8:g.15869353C>A NCBI36
NG_007971.2:g.5532G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.69G>T MANE Select ENSP00000221700.3:p.Leu23=
ENST00000011989.11:c.69G>T ENSP00000011989.8:p.Leu23=
ENST00000221700.10:c.69G>T ENSP00000221700.3:p.Leu23=
ENST00000392846.7:n.49+483G>T
ENST00000586927.2:c.69G>T ENSP00000465514.1:p.Leu23=
ENST00000587671.2:c.69G>T ENSP00000467443.2:p.Leu23=
ENST00000608168.1:n.122G>T
NM_001082.4:c.69G>T NP_001073.3:p.Leu23=
NM_001082.5:c.69G>T MANE Select NP_001073.3:p.Leu23=