Canonical Allele Identifier: CA404579833
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897482T>A , CM000681.2:g.15897482T>A GRCh38
NC_000019.9:g.16008292T>A , CM000681.1:g.16008292T>A GRCh37
NC_000019.8:g.15869292T>A NCBI36
NG_007971.2:g.5593A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.130A>T MANE Select ENSP00000221700.3:p.Asn44Tyr
ENST00000011989.11:c.130A>T ENSP00000011989.8:p.Asn44Tyr
ENST00000221700.10:c.130A>T ENSP00000221700.3:p.Asn44Tyr
ENST00000392846.7:n.49+544A>T
ENST00000586927.2:c.130A>T ENSP00000465514.1:p.Asn44Tyr
ENST00000587671.2:c.130A>T ENSP00000467443.2:p.Asn44Tyr
ENST00000608168.1:n.183A>T
NM_001082.4:c.130A>T NP_001073.3:p.Asn44Tyr
NM_001082.5:c.130A>T MANE Select NP_001073.3:p.Asn44Tyr