Canonical Allele Identifier: CA305861754
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs563639275
gnomAD v3: 19-15640639-C-T
gnomAD v4: 19-15640639-C-T
MyVariant Identifiers: chr19:g.15751449C>T (hg19) chr19:g.15640639C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640639C>T , CM000681.2:g.15640639C>T GRCh38
NC_000019.9:g.15751449C>T , CM000681.1:g.15751449C>T GRCh37
NC_000019.8:g.15612449C>T NCBI36
NG_007964.1:g.4743C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6413C>T ENSP00000478605.1:n.344-6413C>T
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