Canonical Allele Identifier: CA2325096950
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879439G= , CM000681.2:g.15879439G= GRCh38
NC_000019.9:g.15990249G= , CM000681.1:g.15990249G= GRCh37
NC_000019.8:g.15851249G= NCBI36
NG_007971.2:g.23636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315-11C= MANE Select ENSP00000221700.3:n.1315-11C=
ENST00000011989.11:c.1315-11C= ENSP00000011989.8:n.1315-11C=
ENST00000221700.10:c.1315-11C= ENSP00000221700.3:n.1315-11C=
ENST00000392846.7:n.1258-11C=
ENST00000589654.2:c.103-11C=
NM_001082.4:c.1315-11C= NP_001073.3:n.1315-11C=
NM_001082.5:c.1315-11C= MANE Select NP_001073.3:n.1315-11C=
Search 100 bp 5'
Search 100 bp 3'