Canonical Allele Identifier: CA9273650
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs756186873
ExAC: 19:15990229 G / A
gnomAD v2: 19-15990229-G-A
gnomAD v3: 19-15879419-G-A
gnomAD v4: 19-15879419-G-A
MyVariant Identifiers: chr19:g.15990229G>A (hg19) chr19:g.15879419G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879419G>A , CM000681.2:g.15879419G>A GRCh38
NC_000019.9:g.15990229G>A , CM000681.1:g.15990229G>A GRCh37
NC_000019.8:g.15851229G>A NCBI36
NG_007971.2:g.23656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1324C>T MANE Select ENSP00000221700.3:p.Pro442Ser
ENST00000011989.11:c.1324C>T ENSP00000011989.8:p.Pro442Ser
ENST00000221700.10:c.1324C>T ENSP00000221700.3:p.Pro442Ser
ENST00000392846.7:n.1267C>T
ENST00000589654.2:c.112C>T
NM_001082.4:c.1324C>T NP_001073.3:p.Pro442Ser
NM_001082.5:c.1324C>T MANE Select NP_001073.3:p.Pro442Ser
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