Canonical Allele Identifier: CA305879605

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1033087360
• gnomAD v3: 19-15879133-A-C
• gnomAD v4: 19-15879133-A-C
• MyVariant Identifiers: chr19:g.15989943A>C (hg19) ; chr19:g.15879133A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879133A>C , CM000681.2:g.15879133A>C	GRCh38
NC_000019.9:g.15989943A>C , CM000681.1:g.15989943A>C	GRCh37
NC_000019.8:g.15850943A>C	NCBI36
NG_007971.2:g.23942T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1398-197T>G MANE Select	ENSP00000221700.3:n.1398-197T>G
ENST00000011989.11:c.1398-197T>G	ENSP00000011989.8:n.1398-197T>G
ENST00000221700.10:c.1398-197T>G	ENSP00000221700.3:n.1398-197T>G
ENST00000392846.7:n.1341-197T>G
ENST00000589654.2:c.186-197T>G
NM_001082.4:c.1398-197T>G	NP_001073.3:n.1398-197T>G
NM_001082.5:c.1398-197T>G MANE Select	NP_001073.3:n.1398-197T>G