Canonical Allele Identifier: CA2576659150
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897638G>A , CM000681.2:g.15897638G>A GRCh38
NC_000019.9:g.16008448G>A , CM000681.1:g.16008448G>A GRCh37
NC_000019.8:g.15869448G>A NCBI36
NG_007971.2:g.5437C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-26C>T MANE Select ENSP00000221700.3:n.-1-26C>T
ENST00000011989.11:c.-1-26C>T ENSP00000011989.8:n.-1-26C>T
ENST00000221700.10:c.-1-26C>T ENSP00000221700.3:n.-1-26C>T
ENST00000392846.7:n.49+388C>T
ENST00000586927.2:c.-27C>T ENSP00000465514.1:n.-27C>T
ENST00000587671.2:c.-1-26C>T ENSP00000467443.2:n.-1-26C>T
ENST00000608168.1:n.53-26C>T
NM_001082.4:c.-1-26C>T NP_001073.3:n.-1-26C>T
NM_001082.5:c.-1-26C>T MANE Select NP_001073.3:n.-1-26C>T