Canonical Allele Identifier: CA404576000
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16000262C>G (hg19) chr19:g.15889452C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889452C>G , CM000681.2:g.15889452C>G GRCh38
NC_000019.9:g.16000262C>G , CM000681.1:g.16000262C>G GRCh37
NC_000019.8:g.15861262C>G NCBI36
NG_007971.2:g.13623G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.889G>C MANE Select ENSP00000221700.3:p.Asp297His
ENST00000011989.11:c.889G>C ENSP00000011989.8:p.Asp297His
ENST00000221700.10:c.889G>C ENSP00000221700.3:p.Asp297His
ENST00000392846.7:n.832G>C
ENST00000587671.2:c.*474G>C ENSP00000467443.2:n.*474G>C
NM_001082.4:c.889G>C NP_001073.3:p.Asp297His
NM_001082.5:c.889G>C MANE Select NP_001073.3:p.Asp297His
Search 100 bp 5'
Search 100 bp 3'