Canonical Allele Identifier: CA2324940653
Gene: CYP4F23P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15566852T= , CM000681.2:g.15566852T= GRCh38
NC_000019.9:g.15677663T= , CM000681.1:g.15677663T= GRCh37
NC_000019.8:g.15538663T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000593402.6:n.201+2578T=