Canonical Allele Identifier: CA2583119891

Gene: CYP4F3

Linked Data

• gnomAD v4: 19-15641094-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15641094C>G , CM000681.2:g.15641094C>G	GRCh38
NC_000019.9:g.15751904C>G , CM000681.1:g.15751904C>G	GRCh37
NC_000019.8:g.15612904C>G	NCBI36
NG_007964.1:g.5198C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000221307.13:c.-2+149C>G MANE Select	ENSP00000221307.6:n.-2+149C>G
ENST00000221307.12:c.-2+149C>G	ENSP00000221307.6:n.-2+149C>G
ENST00000586182.6:c.-2+165C>G	ENSP00000466395.1:n.-2+165C>G
ENST00000591058.5:c.-2+149C>G	ENSP00000466988.1:n.-2+149C>G
ENST00000592279.6:n.49+149C>G
ENST00000620621.4:c.344-5958C>G	ENSP00000478605.1:n.344-5958C>G
NM_000896.2:c.-2+149C>G	NP_000887.2:n.-2+149C>G
NM_001199208.1:c.-2+149C>G	NP_001186137.1:n.-2+149C>G
NM_001199209.1:c.-2+165C>G	NP_001186138.1:n.-2+165C>G
NM_000896.3:c.-2+149C>G MANE Select	NP_000887.2:n.-2+149C>G
NM_001199208.2:c.-2+149C>G	NP_001186137.1:n.-2+149C>G
NM_001199209.2:c.-2+165C>G	NP_001186138.1:n.-2+165C>G