Canonical Allele Identifier: CA305862024

Gene: CYP4F3

Linked Data

• dbSNP Id: rs887499529
• gnomAD v3: 19-15640954-G-A
• gnomAD v4: 19-15640954-G-A
• MyVariant Identifiers: chr19:g.15640954G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640954G>A , CM000681.2:g.15640954G>A	GRCh38
NC_000019.9:g.15751764G>A , CM000681.1:g.15751764G>A	GRCh37
NC_000019.8:g.15612764G>A	NCBI36
NG_007964.1:g.5058G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-2+9G>A MANE Select	ENSP00000221307.6:n.-2+9G>A
ENST00000221307.12:c.-2+9G>A	ENSP00000221307.6:n.-2+9G>A
ENST00000586182.6:c.-2+25G>A	ENSP00000466395.1:n.-2+25G>A
ENST00000591058.5:c.-2+9G>A	ENSP00000466988.1:n.-2+9G>A
ENST00000592279.6:n.49+9G>A
ENST00000620621.4:c.344-6098G>A	ENSP00000478605.1:n.344-6098G>A
NM_000896.2:c.-2+9G>A	NP_000887.2:n.-2+9G>A
NM_001199208.1:c.-2+9G>A	NP_001186137.1:n.-2+9G>A
NM_001199209.1:c.-2+25G>A	NP_001186138.1:n.-2+25G>A
NM_000896.3:c.-2+9G>A MANE Select	NP_000887.2:n.-2+9G>A
NM_001199208.2:c.-2+9G>A	NP_001186137.1:n.-2+9G>A
NM_001199209.2:c.-2+25G>A	NP_001186138.1:n.-2+25G>A