Canonical Allele Identifier: CA505872659
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1368461658

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897597G>A , CM000681.2:g.15897597G>A GRCh38
NC_000019.9:g.16008407G>A , CM000681.1:g.16008407G>A GRCh37
NC_000019.8:g.15869407G>A NCBI36
NG_007971.2:g.5478C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.15C>T MANE Select ENSP00000221700.3:p.Ser5=
ENST00000011989.11:c.15C>T ENSP00000011989.8:p.Ser5=
ENST00000221700.10:c.15C>T ENSP00000221700.3:p.Ser5=
ENST00000392846.7:n.49+429C>T
ENST00000586927.2:c.15C>T ENSP00000465514.1:p.Ser5=
ENST00000587671.2:c.15C>T ENSP00000467443.2:p.Ser5=
ENST00000608168.1:n.68C>T
NM_001082.4:c.15C>T NP_001073.3:p.Ser5=
NM_001082.5:c.15C>T MANE Select NP_001073.3:p.Ser5=