Canonical Allele Identifier: CA2576659160

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897706-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897706C>T , CM000681.2:g.15897706C>T	GRCh38
NC_000019.9:g.16008516C>T , CM000681.1:g.16008516C>T	GRCh37
NC_000019.8:g.15869516C>T	NCBI36
NG_007971.2:g.5369G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-94G>A MANE Select	ENSP00000221700.3:n.-1-94G>A
ENST00000011989.11:c.-1-94G>A	ENSP00000011989.8:n.-1-94G>A
ENST00000221700.10:c.-1-94G>A	ENSP00000221700.3:n.-1-94G>A
ENST00000392846.7:n.49+320G>A
ENST00000586927.2:c.-95G>A	ENSP00000465514.1:n.-95G>A
ENST00000587671.2:c.-1-94G>A	ENSP00000467443.2:n.-1-94G>A
ENST00000608168.1:n.53-94G>A
NM_001082.4:c.-1-94G>A	NP_001073.3:n.-1-94G>A
NM_001082.5:c.-1-94G>A MANE Select	NP_001073.3:n.-1-94G>A