Canonical Allele Identifier: CA404579767
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1444158492

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897448G>C , CM000681.2:g.15897448G>C GRCh38
NC_000019.9:g.16008258G>C , CM000681.1:g.16008258G>C GRCh37
NC_000019.8:g.15869258G>C NCBI36
NG_007971.2:g.5627C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.164C>G MANE Select ENSP00000221700.3:p.Pro55Arg
ENST00000011989.11:c.164C>G ENSP00000011989.8:p.Pro55Arg
ENST00000221700.10:c.164C>G ENSP00000221700.3:p.Pro55Arg
ENST00000392846.7:n.49+578C>G
ENST00000586927.2:c.164C>G ENSP00000465514.1:p.Pro55Arg
ENST00000587671.2:c.164C>G ENSP00000467443.2:p.Pro55Arg
ENST00000608168.1:n.217C>G
NM_001082.4:c.164C>G NP_001073.3:p.Pro55Arg
NM_001082.5:c.164C>G MANE Select NP_001073.3:p.Pro55Arg