Canonical Allele Identifier: CA2583146238

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15889350-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15889350T>C , CM000681.2:g.15889350T>C	GRCh38
NC_000019.9:g.16000160T>C , CM000681.1:g.16000160T>C	GRCh37
NC_000019.8:g.15861160T>C	NCBI36
NG_007971.2:g.13725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.918+73A>G MANE Select	ENSP00000221700.3:n.918+73A>G
ENST00000011989.11:c.918+73A>G	ENSP00000011989.8:n.918+73A>G
ENST00000221700.10:c.918+73A>G	ENSP00000221700.3:n.918+73A>G
ENST00000392846.7:n.861+73A>G
ENST00000587671.2:c.*503+73A>G	ENSP00000467443.2:n.*503+73A>G
NM_001082.4:c.918+73A>G	NP_001073.3:n.918+73A>G
NM_001082.5:c.918+73A>G MANE Select	NP_001073.3:n.918+73A>G