Canonical Allele Identifier: CA783658267
Gene: CYP4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1475955964
gnomAD v3: 19-15640647-ACT-A
gnomAD v4: 19-15640647-ACT-A
MyVariant Identifiers: chr19:g.15751458_15751459del (hg19) chr19:g.15640648_15640649del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640650_15640651del , CM000681.2:g.15640650_15640651del GRCh38
NC_000019.9:g.15751460_15751461del , CM000681.1:g.15751460_15751461del GRCh37
NC_000019.8:g.15612460_15612461del NCBI36
NG_007964.1:g.4754_4755del

Transcript Alleles

HGVS Amino-acid Change
ENST00000620621.4:c.344-6402_344-6401del ENSP00000478605.1:n.344-6402_344-6401del
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