Canonical Allele Identifier: CA2324940726
Gene: CYP4F23P HGNC NCBI

Linked Data

dbSNP Id: rs1971717623
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15566999C>T , CM000681.2:g.15566999C>T GRCh38
NC_000019.9:g.15677810C>T , CM000681.1:g.15677810C>T GRCh37
NC_000019.8:g.15538810C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000593402.6:n.201+2725C>T
Search 100 bp 5'
Search 100 bp 3'