Canonical Allele Identifier: CA2325101717
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs2089400416

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889162T>A , CM000681.2:g.15889162T>A GRCh38
NC_000019.9:g.15999972T>A , CM000681.1:g.15999972T>A GRCh37
NC_000019.8:g.15860972T>A NCBI36
NG_007971.2:g.13913A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.918+261A>T MANE Select ENSP00000221700.3:n.918+261A>T
ENST00000011989.11:c.918+261A>T ENSP00000011989.8:n.918+261A>T
ENST00000221700.10:c.918+261A>T ENSP00000221700.3:n.918+261A>T
ENST00000392846.7:n.861+261A>T
ENST00000587671.2:c.*503+261A>T ENSP00000467443.2:n.*503+261A>T
NM_001082.4:c.918+261A>T NP_001073.3:n.918+261A>T
NM_001082.5:c.918+261A>T MANE Select NP_001073.3:n.918+261A>T