Canonical Allele Identifier: CA632130290
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1439176244
gnomAD v2: 19-16008455-TG-T
gnomAD v3: 19-15897645-TG-T
gnomAD v4: 19-15897645-TG-T
MyVariant Identifiers: chr19:g.16008456del (hg19) chr19:g.15897646del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897646del , CM000681.2:g.15897646del GRCh38
NC_000019.9:g.16008456del , CM000681.1:g.16008456del GRCh37
NC_000019.8:g.15869456del NCBI36
NG_007971.2:g.5429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-34del MANE Select ENSP00000221700.3:n.-1-34del
ENST00000011989.11:c.-1-34del ENSP00000011989.8:n.-1-34del
ENST00000221700.10:c.-1-34del ENSP00000221700.3:n.-1-34del
ENST00000392846.7:n.49+380del
ENST00000586927.2:c.-35del ENSP00000465514.1:n.-35del
ENST00000587671.2:c.-1-34del ENSP00000467443.2:n.-1-34del
ENST00000608168.1:n.53-34del
NM_001082.4:c.-1-34del NP_001073.3:n.-1-34del
NM_001082.5:c.-1-34del MANE Select NP_001073.3:n.-1-34del
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