Canonical Allele Identifier: CA2324977550
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1290617
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15641087T>C , CM000681.2:g.15641087T>C GRCh38
NC_000019.9:g.15751897T>C , CM000681.1:g.15751897T>C GRCh37
NC_000019.8:g.15612897T>C NCBI36
NG_007964.1:g.5191T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221307.13:c.-2+142T>C MANE Select ENSP00000221307.6:n.-2+142T>C
ENST00000221307.12:c.-2+142T>C ENSP00000221307.6:n.-2+142T>C
ENST00000586182.6:c.-2+158T>C ENSP00000466395.1:n.-2+158T>C
ENST00000591058.5:c.-2+142T>C ENSP00000466988.1:n.-2+142T>C
ENST00000592279.6:n.49+142T>C
ENST00000620621.4:c.344-5965T>C ENSP00000478605.1:n.344-5965T>C
NM_000896.2:c.-2+142T>C NP_000887.2:n.-2+142T>C
NM_001199208.1:c.-2+142T>C NP_001186137.1:n.-2+142T>C
NM_001199209.1:c.-2+158T>C NP_001186138.1:n.-2+158T>C
NM_000896.3:c.-2+142T>C MANE Select NP_000887.2:n.-2+142T>C
NM_001199208.2:c.-2+142T>C NP_001186137.1:n.-2+142T>C
NM_001199209.2:c.-2+158T>C NP_001186138.1:n.-2+158T>C
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