Canonical Allele Identifier: CA305852790

Gene: CYP4F23P

Linked Data

• dbSNP Id: rs562958211
• gnomAD v2: 19-15677799-G-T
• gnomAD v3: 19-15566988-G-T
• gnomAD v4: 19-15566988-G-T
• MyVariant Identifiers: chr19:g.15677799G>T (hg19) ; chr19:g.15566988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15566988G>T , CM000681.2:g.15566988G>T	GRCh38
NC_000019.9:g.15677799G>T , CM000681.1:g.15677799G>T	GRCh37
NC_000019.8:g.15538799G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593402.6:n.201+2714G>T