Canonical Allele Identifier: CA305861815

Gene: CYP4F3

Linked Data

• dbSNP Id: rs951870099
• gnomAD v2: 19-15751551-T-C
• gnomAD v3: 19-15640741-T-C
• gnomAD v4: 19-15640741-T-C
• MyVariant Identifiers: chr19:g.15751551T>C (hg19) ; chr19:g.15640741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640741T>C , CM000681.2:g.15640741T>C	GRCh38
NC_000019.9:g.15751551T>C , CM000681.1:g.15751551T>C	GRCh37
NC_000019.8:g.15612551T>C	NCBI36
NG_007964.1:g.4845T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620621.4:c.344-6311T>C	ENSP00000478605.1:n.344-6311T>C