Canonical Allele Identifier: CA505872519
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16008278A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897468A>G , CM000681.2:g.15897468A>G GRCh38
NC_000019.9:g.16008278A>G , CM000681.1:g.16008278A>G GRCh37
NC_000019.8:g.15869278A>G NCBI36
NG_007971.2:g.5607T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.144T>C MANE Select ENSP00000221700.3:p.Leu48=
ENST00000011989.11:c.144T>C ENSP00000011989.8:p.Leu48=
ENST00000221700.10:c.144T>C ENSP00000221700.3:p.Leu48=
ENST00000392846.7:n.49+558T>C
ENST00000586927.2:c.144T>C ENSP00000465514.1:p.Leu48=
ENST00000587671.2:c.144T>C ENSP00000467443.2:p.Leu48=
ENST00000608168.1:n.197T>C
NM_001082.4:c.144T>C NP_001073.3:p.Leu48=
NM_001082.5:c.144T>C MANE Select NP_001073.3:p.Leu48=