Canonical Allele Identifier: CA2576659148

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897395-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897395A>C , CM000681.2:g.15897395A>C	GRCh38
NC_000019.9:g.16008205A>C , CM000681.1:g.16008205A>C	GRCh37
NC_000019.8:g.15869205A>C	NCBI36
NG_007971.2:g.5680T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+19T>G MANE Select	ENSP00000221700.3:n.198+19T>G
ENST00000011989.11:c.198+19T>G	ENSP00000011989.8:n.198+19T>G
ENST00000221700.10:c.198+19T>G	ENSP00000221700.3:n.198+19T>G
ENST00000392846.7:n.49+631T>G
ENST00000586927.2:c.198+19T>G	ENSP00000465514.1:n.198+19T>G
ENST00000587671.2:c.198+19T>G	ENSP00000467443.2:n.198+19T>G
ENST00000608168.1:n.251+19T>G
NM_001082.4:c.198+19T>G	NP_001073.3:n.198+19T>G
NM_001082.5:c.198+19T>G MANE Select	NP_001073.3:n.198+19T>G