Canonical Allele Identifier: CA404572749
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879410A>C , CM000681.2:g.15879410A>C GRCh38
NC_000019.9:g.15990220A>C , CM000681.1:g.15990220A>C GRCh37
NC_000019.8:g.15851220A>C NCBI36
NG_007971.2:g.23665T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1333T>G MANE Select ENSP00000221700.3:p.Phe445Val
ENST00000011989.11:c.1333T>G ENSP00000011989.8:p.Phe445Val
ENST00000221700.10:c.1333T>G ENSP00000221700.3:p.Phe445Val
ENST00000392846.7:n.1276T>G
ENST00000589654.2:c.121T>G
NM_001082.4:c.1333T>G NP_001073.3:p.Phe445Val
NM_001082.5:c.1333T>G MANE Select NP_001073.3:p.Phe445Val