Canonical Allele Identifier: CA404579694

Gene: CYP4F2

Linked Data

• dbSNP Id: rs2089453953
• gnomAD v3: 19-15897414-C-T
• gnomAD v4: 19-15897414-C-T
• MyVariant Identifiers: chr19:g.16008224C>T (hg19) ; chr19:g.15897414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897414C>T , CM000681.2:g.15897414C>T	GRCh38
NC_000019.9:g.16008224C>T , CM000681.1:g.16008224C>T	GRCh37
NC_000019.8:g.15869224C>T	NCBI36
NG_007971.2:g.5661G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198G>A MANE Select	ENSP00000221700.3:p.Met66Ile
ENST00000011989.11:c.198G>A	ENSP00000011989.8:p.Met66Ile
ENST00000221700.10:c.198G>A	ENSP00000221700.3:p.Met66Ile
ENST00000392846.7:n.49+612G>A
ENST00000586927.2:c.198G>A	ENSP00000465514.1:p.Met66Ile
ENST00000587671.2:c.198G>A	ENSP00000467443.2:p.Met66Ile
ENST00000608168.1:n.251G>A
NM_001082.4:c.198G>A	NP_001073.3:p.Met66Ile
NM_001082.5:c.198G>A MANE Select	NP_001073.3:p.Met66Ile