Canonical Allele Identifier: CA2324977517
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1972447104

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15641023C>T , CM000681.2:g.15641023C>T GRCh38
NC_000019.9:g.15751833C>T , CM000681.1:g.15751833C>T GRCh37
NC_000019.8:g.15612833C>T NCBI36
NG_007964.1:g.5127C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221307.13:c.-2+78C>T MANE Select ENSP00000221307.6:n.-2+78C>T
ENST00000221307.12:c.-2+78C>T ENSP00000221307.6:n.-2+78C>T
ENST00000586182.6:c.-2+94C>T ENSP00000466395.1:n.-2+94C>T
ENST00000591058.5:c.-2+78C>T ENSP00000466988.1:n.-2+78C>T
ENST00000592279.6:n.49+78C>T
ENST00000620621.4:c.344-6029C>T ENSP00000478605.1:n.344-6029C>T
NM_000896.2:c.-2+78C>T NP_000887.2:n.-2+78C>T
NM_001199208.1:c.-2+78C>T NP_001186137.1:n.-2+78C>T
NM_001199209.1:c.-2+94C>T NP_001186138.1:n.-2+94C>T
NM_000896.3:c.-2+78C>T MANE Select NP_000887.2:n.-2+78C>T
NM_001199208.2:c.-2+78C>T NP_001186137.1:n.-2+78C>T
NM_001199209.2:c.-2+94C>T NP_001186138.1:n.-2+94C>T