Canonical Allele Identifier: CA305861945

Gene: CYP4F3

Linked Data

• dbSNP Id: rs945013388
• gnomAD v4: 19-15640876-G-A
• MyVariant Identifiers: chr19:g.15751686G>A (hg19) ; chr19:g.15640876G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640876G>A , CM000681.2:g.15640876G>A	GRCh38
NC_000019.9:g.15751686G>A , CM000681.1:g.15751686G>A	GRCh37
NC_000019.8:g.15612686G>A	NCBI36
NG_007964.1:g.4980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6176G>A	ENSP00000478605.1:n.344-6176G>A