Canonical Allele Identifier: CA783662220

Gene: CYP4F23P

Linked Data

• dbSNP Id: rs1273516
• gnomAD v3: 19-15566899-G-C
• gnomAD v4: 19-15566899-G-C
• MyVariant Identifiers: chr19:g.15677710G>C (hg19) ; chr19:g.15566899G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15566899G>C , CM000681.2:g.15566899G>C	GRCh38
NC_000019.9:g.15677710G>C , CM000681.1:g.15677710G>C	GRCh37
NC_000019.8:g.15538710G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000593402.6:n.201+2625G>C