Canonical Allele Identifier: CA404572852
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15990238C>T (hg19) chr19:g.15879428C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879428C>T , CM000681.2:g.15879428C>T GRCh38
NC_000019.9:g.15990238C>T , CM000681.1:g.15990238C>T GRCh37
NC_000019.8:g.15851238C>T NCBI36
NG_007971.2:g.23647G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315G>A MANE Select ENSP00000221700.3:p.Val439Ile
ENST00000011989.11:c.1315G>A ENSP00000011989.8:p.Val439Ile
ENST00000221700.10:c.1315G>A ENSP00000221700.3:p.Val439Ile
ENST00000392846.7:n.1258G>A
ENST00000589654.2:c.103G>A
NM_001082.4:c.1315G>A NP_001073.3:p.Val439Ile
NM_001082.5:c.1315G>A MANE Select NP_001073.3:p.Val439Ile
Search 100 bp 5'
Search 100 bp 3'