Canonical Allele Identifier: CA783658535
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1291711417
gnomAD v4: 19-15641093-G-A
MyVariant Identifiers: chr19:g.15751903G>A (hg19) chr19:g.15641093G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15641093G>A , CM000681.2:g.15641093G>A GRCh38
NC_000019.9:g.15751903G>A , CM000681.1:g.15751903G>A GRCh37
NC_000019.8:g.15612903G>A NCBI36
NG_007964.1:g.5197G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221307.13:c.-2+148G>A MANE Select ENSP00000221307.6:n.-2+148G>A
ENST00000221307.12:c.-2+148G>A ENSP00000221307.6:n.-2+148G>A
ENST00000586182.6:c.-2+164G>A ENSP00000466395.1:n.-2+164G>A
ENST00000591058.5:c.-2+148G>A ENSP00000466988.1:n.-2+148G>A
ENST00000592279.6:n.49+148G>A
ENST00000620621.4:c.344-5959G>A ENSP00000478605.1:n.344-5959G>A
NM_000896.2:c.-2+148G>A NP_000887.2:n.-2+148G>A
NM_001199208.1:c.-2+148G>A NP_001186137.1:n.-2+148G>A
NM_001199209.1:c.-2+164G>A NP_001186138.1:n.-2+164G>A
NM_000896.3:c.-2+148G>A MANE Select NP_000887.2:n.-2+148G>A
NM_001199208.2:c.-2+148G>A NP_001186137.1:n.-2+148G>A
NM_001199209.2:c.-2+164G>A NP_001186138.1:n.-2+164G>A
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