Canonical Allele Identifier: CA2583119885

Gene: CYP4F3

Linked Data

• gnomAD v4: 19-15641091-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15641091T>C , CM000681.2:g.15641091T>C	GRCh38
NC_000019.9:g.15751901T>C , CM000681.1:g.15751901T>C	GRCh37
NC_000019.8:g.15612901T>C	NCBI36
NG_007964.1:g.5195T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000221307.13:c.-2+146T>C MANE Select	ENSP00000221307.6:n.-2+146T>C
ENST00000221307.12:c.-2+146T>C	ENSP00000221307.6:n.-2+146T>C
ENST00000586182.6:c.-2+162T>C	ENSP00000466395.1:n.-2+162T>C
ENST00000591058.5:c.-2+146T>C	ENSP00000466988.1:n.-2+146T>C
ENST00000592279.6:n.49+146T>C
ENST00000620621.4:c.344-5961T>C	ENSP00000478605.1:n.344-5961T>C
NM_000896.2:c.-2+146T>C	NP_000887.2:n.-2+146T>C
NM_001199208.1:c.-2+146T>C	NP_001186137.1:n.-2+146T>C
NM_001199209.1:c.-2+162T>C	NP_001186138.1:n.-2+162T>C
NM_000896.3:c.-2+146T>C MANE Select	NP_000887.2:n.-2+146T>C
NM_001199208.2:c.-2+146T>C	NP_001186137.1:n.-2+146T>C
NM_001199209.2:c.-2+162T>C	NP_001186138.1:n.-2+162T>C