Canonical Allele Identifier: CA305861907

Gene: CYP4F3

Linked Data

• dbSNP Id: rs889271590
• gnomAD v2: 19-15751669-G-T
• gnomAD v3: 19-15640859-G-T
• gnomAD v4: 19-15640859-G-T
• MyVariant Identifiers: chr19:g.15751669G>T (hg19) ; chr19:g.15640859G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640859G>T , CM000681.2:g.15640859G>T	GRCh38
NC_000019.9:g.15751669G>T , CM000681.1:g.15751669G>T	GRCh37
NC_000019.8:g.15612669G>T	NCBI36
NG_007964.1:g.4963G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6193G>T	ENSP00000478605.1:n.344-6193G>T