Canonical Allele Identifier: CA404579734
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16008242A>C (hg19) chr19:g.15897432A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897432A>C , CM000681.2:g.15897432A>C GRCh38
NC_000019.9:g.16008242A>C , CM000681.1:g.16008242A>C GRCh37
NC_000019.8:g.15869242A>C NCBI36
NG_007971.2:g.5643T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.180T>G MANE Select ENSP00000221700.3:p.Phe60Leu
ENST00000011989.11:c.180T>G ENSP00000011989.8:p.Phe60Leu
ENST00000221700.10:c.180T>G ENSP00000221700.3:p.Phe60Leu
ENST00000392846.7:n.49+594T>G
ENST00000586927.2:c.180T>G ENSP00000465514.1:p.Phe60Leu
ENST00000587671.2:c.180T>G ENSP00000467443.2:p.Phe60Leu
ENST00000608168.1:n.233T>G
NM_001082.4:c.180T>G NP_001073.3:p.Phe60Leu
NM_001082.5:c.180T>G MANE Select NP_001073.3:p.Phe60Leu
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