Canonical Allele Identifier: CA506084555
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16000248T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889438T>G , CM000681.2:g.15889438T>G GRCh38
NC_000019.9:g.16000248T>G , CM000681.1:g.16000248T>G GRCh37
NC_000019.8:g.15861248T>G NCBI36
NG_007971.2:g.13637A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.903A>C MANE Select ENSP00000221700.3:p.Val301=
ENST00000011989.11:c.903A>C ENSP00000011989.8:p.Val301=
ENST00000221700.10:c.903A>C ENSP00000221700.3:p.Val301=
ENST00000392846.7:n.846A>C
ENST00000587671.2:c.*488A>C ENSP00000467443.2:n.*488A>C
NM_001082.4:c.903A>C NP_001073.3:p.Val301=
NM_001082.5:c.903A>C MANE Select NP_001073.3:p.Val301=
Search 100 bp 5'
Search 100 bp 3'