Canonical Allele Identifier: CA2557006452
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879136G>A , CM000681.2:g.15879136G>A GRCh38
NC_000019.9:g.15989946G>A , CM000681.1:g.15989946G>A GRCh37
NC_000019.8:g.15850946G>A NCBI36
NG_007971.2:g.23939C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1398-200C>T MANE Select ENSP00000221700.3:n.1398-200C>T
ENST00000011989.11:c.1398-200C>T ENSP00000011989.8:n.1398-200C>T
ENST00000221700.10:c.1398-200C>T ENSP00000221700.3:n.1398-200C>T
ENST00000392846.7:n.1341-200C>T
ENST00000589654.2:c.186-200C>T
NM_001082.4:c.1398-200C>T NP_001073.3:n.1398-200C>T
NM_001082.5:c.1398-200C>T MANE Select NP_001073.3:n.1398-200C>T