Canonical Allele Identifier: CA783658326

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1266094651
• MyVariant Identifiers: chr19:g.15751568G>C (hg19) ; chr19:g.15640758G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640758G>C , CM000681.2:g.15640758G>C	GRCh38
NC_000019.9:g.15751568G>C , CM000681.1:g.15751568G>C	GRCh37
NC_000019.8:g.15612568G>C	NCBI36
NG_007964.1:g.4862G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6294G>C	ENSP00000478605.1:n.344-6294G>C