Canonical Allele Identifier: CA305852695

Gene: CYP4F23P

Linked Data

• dbSNP Id: rs558152173
• gnomAD v3: 19-15566851-A-G
• gnomAD v4: 19-15566851-A-G
• MyVariant Identifiers: chr19:g.15677662A>G (hg19) ; chr19:g.15566851A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15566851A>G , CM000681.2:g.15566851A>G	GRCh38
NC_000019.9:g.15677662A>G , CM000681.1:g.15677662A>G	GRCh37
NC_000019.8:g.15538662A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593402.6:n.201+2577A>G