Canonical Allele Identifier: CA404572540
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs2089328206
MyVariant Identifiers: chr19:g.15990168G>T (hg19) chr19:g.15879358G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879358G>T , CM000681.2:g.15879358G>T GRCh38
NC_000019.9:g.15990168G>T , CM000681.1:g.15990168G>T GRCh37
NC_000019.8:g.15851168G>T NCBI36
NG_007971.2:g.23717C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1385C>A MANE Select ENSP00000221700.3:p.Ser462Ter
ENST00000011989.11:c.1385C>A ENSP00000011989.8:p.Ser462Ter
ENST00000221700.10:c.1385C>A ENSP00000221700.3:p.Ser462Ter
ENST00000392846.7:n.1328C>A
ENST00000589654.2:c.173C>A
NM_001082.4:c.1385C>A NP_001073.3:p.Ser462Ter
NM_001082.5:c.1385C>A MANE Select NP_001073.3:p.Ser462Ter
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