Canonical Allele Identifier: CA404579826
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16008289A>G (hg19) chr19:g.15897479A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897479A>G , CM000681.2:g.15897479A>G GRCh38
NC_000019.9:g.16008289A>G , CM000681.1:g.16008289A>G GRCh37
NC_000019.8:g.15869289A>G NCBI36
NG_007971.2:g.5596T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.133T>C MANE Select ENSP00000221700.3:p.Cys45Arg
ENST00000011989.11:c.133T>C ENSP00000011989.8:p.Cys45Arg
ENST00000221700.10:c.133T>C ENSP00000221700.3:p.Cys45Arg
ENST00000392846.7:n.49+547T>C
ENST00000586927.2:c.133T>C ENSP00000465514.1:p.Cys45Arg
ENST00000587671.2:c.133T>C ENSP00000467443.2:p.Cys45Arg
ENST00000608168.1:n.186T>C
NM_001082.4:c.133T>C NP_001073.3:p.Cys45Arg
NM_001082.5:c.133T>C MANE Select NP_001073.3:p.Cys45Arg
Search 100 bp 5'
Search 100 bp 3'