Canonical Allele Identifier: CA305909874
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs2906891

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897576C>G , CM000681.2:g.15897576C>G GRCh38
NC_000019.9:g.16008386C>G , CM000681.1:g.16008386C>G GRCh37
NC_000019.8:g.15869386C>G NCBI36
NG_007971.2:g.5499G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.36G>C MANE Select ENSP00000221700.3:p.Trp12Cys
ENST00000011989.11:c.36G>C ENSP00000011989.8:p.Trp12Cys
ENST00000221700.10:c.36G>C ENSP00000221700.3:p.Trp12Cys
ENST00000392846.7:n.49+450G>C
ENST00000586927.2:c.36G>C ENSP00000465514.1:p.Trp12Cys
ENST00000587671.2:c.36G>C ENSP00000467443.2:p.Trp12Cys
ENST00000608168.1:n.89G>C
NM_001082.4:c.36G>C NP_001073.3:p.Trp12Cys
NM_001082.5:c.36G>C MANE Select NP_001073.3:p.Trp12Cys