Canonical Allele Identifier: CA2735697205

Gene: CYP4F2

Linked Data

• dbSNP Id: rs2145018046

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897657A>T , CM000681.2:g.15897657A>T	GRCh38
NC_000019.9:g.16008467A>T , CM000681.1:g.16008467A>T	GRCh37
NC_000019.8:g.15869467A>T	NCBI36
NG_007971.2:g.5418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-45T>A MANE Select	ENSP00000221700.3:n.-1-45T>A
ENST00000011989.11:c.-1-45T>A	ENSP00000011989.8:n.-1-45T>A
ENST00000221700.10:c.-1-45T>A	ENSP00000221700.3:n.-1-45T>A
ENST00000392846.7:n.49+369T>A
ENST00000586927.2:c.-46T>A	ENSP00000465514.1:n.-46T>A
ENST00000587671.2:c.-1-45T>A	ENSP00000467443.2:n.-1-45T>A
ENST00000608168.1:n.53-45T>A
NM_001082.4:c.-1-45T>A	NP_001073.3:n.-1-45T>A
NM_001082.5:c.-1-45T>A MANE Select	NP_001073.3:n.-1-45T>A