Canonical Allele Identifier: CA783658544

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1220842544
• gnomAD v3: 19-15641108-G-T
• gnomAD v4: 19-15641108-G-T
• MyVariant Identifiers: chr19:g.15751918G>T (hg19) ; chr19:g.15641108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15641108G>T , CM000681.2:g.15641108G>T	GRCh38
NC_000019.9:g.15751918G>T , CM000681.1:g.15751918G>T	GRCh37
NC_000019.8:g.15612918G>T	NCBI36
NG_007964.1:g.5212G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000221307.13:c.-2+163G>T MANE Select	ENSP00000221307.6:n.-2+163G>T
ENST00000221307.12:c.-2+163G>T	ENSP00000221307.6:n.-2+163G>T
ENST00000586182.6:c.-2+179G>T	ENSP00000466395.1:n.-2+179G>T
ENST00000591058.5:c.-2+163G>T	ENSP00000466988.1:n.-2+163G>T
ENST00000592279.6:n.49+163G>T
ENST00000620621.4:c.344-5944G>T	ENSP00000478605.1:n.344-5944G>T
NM_000896.2:c.-2+163G>T	NP_000887.2:n.-2+163G>T
NM_001199208.1:c.-2+163G>T	NP_001186137.1:n.-2+163G>T
NM_001199209.1:c.-2+179G>T	NP_001186138.1:n.-2+179G>T
NM_000896.3:c.-2+163G>T MANE Select	NP_000887.2:n.-2+163G>T
NM_001199208.2:c.-2+163G>T	NP_001186137.1:n.-2+163G>T
NM_001199209.2:c.-2+179G>T	NP_001186138.1:n.-2+179G>T