Canonical Allele Identifier: CA631961364

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1227529717
• gnomAD v2: 19-15751494-T-A
• gnomAD v3: 19-15640684-T-A
• gnomAD v4: 19-15640684-T-A
• MyVariant Identifiers: chr19:g.15751494T>A (hg19) ; chr19:g.15640684T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640684T>A , CM000681.2:g.15640684T>A	GRCh38
NC_000019.9:g.15751494T>A , CM000681.1:g.15751494T>A	GRCh37
NC_000019.8:g.15612494T>A	NCBI36
NG_007964.1:g.4788T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6368T>A	ENSP00000478605.1:n.344-6368T>A