Canonical Allele Identifier: CA505869044
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15990185C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879375C>A , CM000681.2:g.15879375C>A GRCh38
NC_000019.9:g.15990185C>A , CM000681.1:g.15990185C>A GRCh37
NC_000019.8:g.15851185C>A NCBI36
NG_007971.2:g.23700G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1368G>T MANE Select ENSP00000221700.3:p.Leu456=
ENST00000011989.11:c.1368G>T ENSP00000011989.8:p.Leu456=
ENST00000221700.10:c.1368G>T ENSP00000221700.3:p.Leu456=
ENST00000392846.7:n.1311G>T
ENST00000589654.2:c.156G>T
NM_001082.4:c.1368G>T NP_001073.3:p.Leu456=
NM_001082.5:c.1368G>T MANE Select NP_001073.3:p.Leu456=
Search 100 bp 5'
Search 100 bp 3'