Canonical Allele Identifier: CA783658304
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs897489654
gnomAD v3: 19-15640691-G-C
gnomAD v4: 19-15640691-G-C
MyVariant Identifiers: chr19:g.15751501G>C (hg19) chr19:g.15640691G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640691G>C , CM000681.2:g.15640691G>C GRCh38
NC_000019.9:g.15751501G>C , CM000681.1:g.15751501G>C GRCh37
NC_000019.8:g.15612501G>C NCBI36
NG_007964.1:g.4795G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6361G>C ENSP00000478605.1:n.344-6361G>C
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