Canonical Allele Identifier: CA404575957
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16000243A>T (hg19) chr19:g.15889433A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889433A>T , CM000681.2:g.15889433A>T GRCh38
NC_000019.9:g.16000243A>T , CM000681.1:g.16000243A>T GRCh37
NC_000019.8:g.15861243A>T NCBI36
NG_007971.2:g.13642T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.908T>A MANE Select ENSP00000221700.3:p.Leu303Gln
ENST00000011989.11:c.908T>A ENSP00000011989.8:p.Leu303Gln
ENST00000221700.10:c.908T>A ENSP00000221700.3:p.Leu303Gln
ENST00000392846.7:n.851T>A
ENST00000587671.2:c.*493T>A ENSP00000467443.2:n.*493T>A
NM_001082.4:c.908T>A NP_001073.3:p.Leu303Gln
NM_001082.5:c.908T>A MANE Select NP_001073.3:p.Leu303Gln
Search 100 bp 5'
Search 100 bp 3'