Canonical Allele Identifier: CA305861808

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1027371086
• gnomAD v2: 19-15751521-C-T
• MyVariant Identifiers: chr19:g.15751521C>T (hg19) ; chr19:g.15640711C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640711C>T , CM000681.2:g.15640711C>T	GRCh38
NC_000019.9:g.15751521C>T , CM000681.1:g.15751521C>T	GRCh37
NC_000019.8:g.15612521C>T	NCBI36
NG_007964.1:g.4815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6341C>T	ENSP00000478605.1:n.344-6341C>T