Canonical Allele Identifier: CA305861772
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs529479255
gnomAD v3: 19-15640686-TG-T
gnomAD v4: 19-15640686-TG-T
MyVariant Identifiers: chr19:g.15751497del (hg19) chr19:g.15640687del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640689del , CM000681.2:g.15640689del GRCh38
NC_000019.9:g.15751499del , CM000681.1:g.15751499del GRCh37
NC_000019.8:g.15612499del NCBI36
NG_007964.1:g.4793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6363del ENSP00000478605.1:n.344-6363del
Search 100 bp 5'
Search 100 bp 3'