Canonical Allele Identifier: CA9274182
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs3093105

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897578A>C , CM000681.2:g.15897578A>C GRCh38
NC_000019.9:g.16008388A>C , CM000681.1:g.16008388A>C GRCh37
NC_000019.8:g.15869388A>C NCBI36
NG_007971.2:g.5497T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.34T>G MANE Select ENSP00000221700.3:p.Trp12Gly
ENST00000011989.11:c.34T>G ENSP00000011989.8:p.Trp12Gly
ENST00000221700.10:c.34T>G ENSP00000221700.3:p.Trp12Gly
ENST00000392846.7:n.49+448T>G
ENST00000586927.2:c.34T>G ENSP00000465514.1:p.Trp12Gly
ENST00000587671.2:c.34T>G ENSP00000467443.2:p.Trp12Gly
ENST00000608168.1:n.87T>G
NM_001082.4:c.34T>G NP_001073.3:p.Trp12Gly
NM_001082.5:c.34T>G MANE Select NP_001073.3:p.Trp12Gly