Canonical Allele Identifier: CA2813750569

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15889301C>G , CM000681.2:g.15889301C>G	GRCh38
NC_000019.9:g.16000111C>G , CM000681.1:g.16000111C>G	GRCh37
NC_000019.8:g.15861111C>G	NCBI36
NG_007971.2:g.13774G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.918+122G>C MANE Select	ENSP00000221700.3:n.918+122G>C
ENST00000011989.11:c.918+122G>C	ENSP00000011989.8:n.918+122G>C
ENST00000221700.10:c.918+122G>C	ENSP00000221700.3:n.918+122G>C
ENST00000392846.7:n.861+122G>C
ENST00000587671.2:c.*503+122G>C	ENSP00000467443.2:n.*503+122G>C
NM_001082.4:c.918+122G>C	NP_001073.3:n.918+122G>C
NM_001082.5:c.918+122G>C MANE Select	NP_001073.3:n.918+122G>C