Canonical Allele Identifier: CA305861802

Gene: CYP4F3

Linked Data

• dbSNP Id: rs774716874
• gnomAD v3: 19-15640702-C-G
• gnomAD v4: 19-15640702-C-G
• MyVariant Identifiers: chr19:g.15751512C>G (hg19) ; chr19:g.15640702C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640702C>G , CM000681.2:g.15640702C>G	GRCh38
NC_000019.9:g.15751512C>G , CM000681.1:g.15751512C>G	GRCh37
NC_000019.8:g.15612512C>G	NCBI36
NG_007964.1:g.4806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6350C>G	ENSP00000478605.1:n.344-6350C>G