Canonical Allele Identifier: CA305861969

Gene: CYP4F3

Linked Data

• dbSNP Id: rs538511258
• gnomAD v2: 19-15751718-A-C
• gnomAD v3: 19-15640908-A-C
• gnomAD v4: 19-15640908-A-C
• MyVariant Identifiers: chr19:g.15751718A>C (hg19) ; chr19:g.15640908A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640908A>C , CM000681.2:g.15640908A>C	GRCh38
NC_000019.9:g.15751718A>C , CM000681.1:g.15751718A>C	GRCh37
NC_000019.8:g.15612718A>C	NCBI36
NG_007964.1:g.5012A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000221307.13:c.-39A>C MANE Select	ENSP00000221307.6:n.-39A>C
ENST00000221307.12:c.-39A>C	ENSP00000221307.6:n.-39A>C
ENST00000586182.6:c.-23A>C	ENSP00000466395.1:n.-23A>C
ENST00000591058.5:c.-39A>C	ENSP00000466988.1:n.-39A>C
ENST00000592279.6:n.12A>C
ENST00000620621.4:c.344-6144A>C	ENSP00000478605.1:n.344-6144A>C
NM_000896.2:c.-39A>C	NP_000887.2:n.-39A>C
NM_001199208.1:c.-39A>C	NP_001186137.1:n.-39A>C
NM_001199209.1:c.-23A>C	NP_001186138.1:n.-23A>C
NM_000896.3:c.-39A>C MANE Select	NP_000887.2:n.-39A>C
NM_001199208.2:c.-39A>C	NP_001186137.1:n.-39A>C
NM_001199209.2:c.-23A>C	NP_001186138.1:n.-23A>C