Canonical Allele Identifier: CA404579725
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897428C>T , CM000681.2:g.15897428C>T GRCh38
NC_000019.9:g.16008238C>T , CM000681.1:g.16008238C>T GRCh37
NC_000019.8:g.15869238C>T NCBI36
NG_007971.2:g.5647G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.184G>A MANE Select ENSP00000221700.3:p.Gly62Arg
ENST00000011989.11:c.184G>A ENSP00000011989.8:p.Gly62Arg
ENST00000221700.10:c.184G>A ENSP00000221700.3:p.Gly62Arg
ENST00000392846.7:n.49+598G>A
ENST00000586927.2:c.184G>A ENSP00000465514.1:p.Gly62Arg
ENST00000587671.2:c.184G>A ENSP00000467443.2:p.Gly62Arg
ENST00000608168.1:n.237G>A
NM_001082.4:c.184G>A NP_001073.3:p.Gly62Arg
NM_001082.5:c.184G>A MANE Select NP_001073.3:p.Gly62Arg