Canonical Allele Identifier: CA631973741
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1303046687
gnomAD v2: 19-15990041-GA-G
gnomAD v3: 19-15879231-GA-G
gnomAD v4: 19-15879231-GA-G
MyVariant Identifiers: chr19:g.15990042del (hg19) chr19:g.15879232del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879232del , CM000681.2:g.15879232del GRCh38
NC_000019.9:g.15990042del , CM000681.1:g.15990042del GRCh37
NC_000019.8:g.15851042del NCBI36
NG_007971.2:g.23843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+114del MANE Select ENSP00000221700.3:n.1397+114del
ENST00000011989.11:c.1397+114del ENSP00000011989.8:n.1397+114del
ENST00000221700.10:c.1397+114del ENSP00000221700.3:n.1397+114del
ENST00000392846.7:n.1340+114del
ENST00000589654.2:c.185+114del
NM_001082.4:c.1397+114del NP_001073.3:n.1397+114del
NM_001082.5:c.1397+114del MANE Select NP_001073.3:n.1397+114del
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