Canonical Allele Identifier: CA783658305
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1284161725
gnomAD v3: 19-15640696-T-C
gnomAD v4: 19-15640696-T-C
MyVariant Identifiers: chr19:g.15751506T>C (hg19) chr19:g.15640696T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640696T>C , CM000681.2:g.15640696T>C GRCh38
NC_000019.9:g.15751506T>C , CM000681.1:g.15751506T>C GRCh37
NC_000019.8:g.15612506T>C NCBI36
NG_007964.1:g.4800T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6356T>C ENSP00000478605.1:n.344-6356T>C
Search 100 bp 5'
Search 100 bp 3'