Canonical Allele Identifier: CA404572657
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15990198T>G (hg19) chr19:g.15879388T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879388T>G , CM000681.2:g.15879388T>G GRCh38
NC_000019.9:g.15990198T>G , CM000681.1:g.15990198T>G GRCh37
NC_000019.8:g.15851198T>G NCBI36
NG_007971.2:g.23687A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1355A>C MANE Select ENSP00000221700.3:p.Glu452Ala
ENST00000011989.11:c.1355A>C ENSP00000011989.8:p.Glu452Ala
ENST00000221700.10:c.1355A>C ENSP00000221700.3:p.Glu452Ala
ENST00000392846.7:n.1298A>C
ENST00000589654.2:c.143A>C
NM_001082.4:c.1355A>C NP_001073.3:p.Glu452Ala
NM_001082.5:c.1355A>C MANE Select NP_001073.3:p.Glu452Ala
Search 100 bp 5'
Search 100 bp 3'