Canonical Allele Identifier: CA783658469

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1406547509
• gnomAD v4: 19-15640921-T-C
• MyVariant Identifiers: chr19:g.15751731T>C (hg19) ; chr19:g.15640921T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640921T>C , CM000681.2:g.15640921T>C	GRCh38
NC_000019.9:g.15751731T>C , CM000681.1:g.15751731T>C	GRCh37
NC_000019.8:g.15612731T>C	NCBI36
NG_007964.1:g.5025T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-26T>C MANE Select	ENSP00000221307.6:n.-26T>C
ENST00000221307.12:c.-26T>C	ENSP00000221307.6:n.-26T>C
ENST00000586182.6:c.-10T>C	ENSP00000466395.1:n.-10T>C
ENST00000591058.5:c.-26T>C	ENSP00000466988.1:n.-26T>C
ENST00000592279.6:n.25T>C
ENST00000620621.4:c.344-6131T>C	ENSP00000478605.1:n.344-6131T>C
NM_000896.2:c.-26T>C	NP_000887.2:n.-26T>C
NM_001199208.1:c.-26T>C	NP_001186137.1:n.-26T>C
NM_001199209.1:c.-10T>C	NP_001186138.1:n.-10T>C
NM_000896.3:c.-26T>C MANE Select	NP_000887.2:n.-26T>C
NM_001199208.2:c.-26T>C	NP_001186137.1:n.-26T>C
NM_001199209.2:c.-10T>C	NP_001186138.1:n.-10T>C