Canonical Allele Identifier: CA2583119669

Gene: CYP4F3

Linked Data

• gnomAD v4: 19-15640916-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640916T>G , CM000681.2:g.15640916T>G	GRCh38
NC_000019.9:g.15751726T>G , CM000681.1:g.15751726T>G	GRCh37
NC_000019.8:g.15612726T>G	NCBI36
NG_007964.1:g.5020T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-31T>G MANE Select	ENSP00000221307.6:n.-31T>G
ENST00000221307.12:c.-31T>G	ENSP00000221307.6:n.-31T>G
ENST00000586182.6:c.-15T>G	ENSP00000466395.1:n.-15T>G
ENST00000591058.5:c.-31T>G	ENSP00000466988.1:n.-31T>G
ENST00000592279.6:n.20T>G
ENST00000620621.4:c.344-6136T>G	ENSP00000478605.1:n.344-6136T>G
NM_000896.2:c.-31T>G	NP_000887.2:n.-31T>G
NM_001199208.1:c.-31T>G	NP_001186137.1:n.-31T>G
NM_001199209.1:c.-15T>G	NP_001186138.1:n.-15T>G
NM_000896.3:c.-31T>G MANE Select	NP_000887.2:n.-31T>G
NM_001199208.2:c.-31T>G	NP_001186137.1:n.-31T>G
NM_001199209.2:c.-15T>G	NP_001186138.1:n.-15T>G