Canonical Allele Identifier: CA631973736
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1256662538
gnomAD v2: 19-15989942-C-T
gnomAD v3: 19-15879132-C-T
gnomAD v4: 19-15879132-C-T
MyVariant Identifiers: chr19:g.15989942C>T (hg19) chr19:g.15879132C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879132C>T , CM000681.2:g.15879132C>T GRCh38
NC_000019.9:g.15989942C>T , CM000681.1:g.15989942C>T GRCh37
NC_000019.8:g.15850942C>T NCBI36
NG_007971.2:g.23943G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1398-196G>A MANE Select ENSP00000221700.3:n.1398-196G>A
ENST00000011989.11:c.1398-196G>A ENSP00000011989.8:n.1398-196G>A
ENST00000221700.10:c.1398-196G>A ENSP00000221700.3:n.1398-196G>A
ENST00000392846.7:n.1341-196G>A
ENST00000589654.2:c.186-196G>A
NM_001082.4:c.1398-196G>A NP_001073.3:n.1398-196G>A
NM_001082.5:c.1398-196G>A MANE Select NP_001073.3:n.1398-196G>A
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