Canonical Allele Identifier: CA993965779

Gene: CYP4F2

Linked Data

• dbSNP Id: rs2089452660
• gnomAD v3: 19-15897162-A-G
• gnomAD v4: 19-15897162-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897162A>G , CM000681.2:g.15897162A>G	GRCh38
NC_000019.9:g.16007972A>G , CM000681.1:g.16007972A>G	GRCh37
NC_000019.8:g.15868972A>G	NCBI36
NG_007971.2:g.5913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+252T>C MANE Select	ENSP00000221700.3:n.198+252T>C
ENST00000011989.11:c.198+252T>C	ENSP00000011989.8:n.198+252T>C
ENST00000221700.10:c.198+252T>C	ENSP00000221700.3:n.198+252T>C
ENST00000392846.7:n.49+864T>C
ENST00000586927.2:c.198+252T>C	ENSP00000465514.1:n.198+252T>C
ENST00000587671.2:c.198+252T>C	ENSP00000467443.2:n.198+252T>C
ENST00000608168.1:n.251+252T>C
NM_001082.4:c.198+252T>C	NP_001073.3:n.198+252T>C
NM_001082.5:c.198+252T>C MANE Select	NP_001073.3:n.198+252T>C