Canonical Allele Identifier: CA404580068

Gene: CYP4F2

Linked Data

• MyVariant Identifiers: chr19:g.16008413C>A (hg19) ; chr19:g.15897603C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897603C>A , CM000681.2:g.15897603C>A	GRCh38
NC_000019.9:g.16008413C>A , CM000681.1:g.16008413C>A	GRCh37
NC_000019.8:g.15869413C>A	NCBI36
NG_007971.2:g.5472G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.9G>T MANE Select	ENSP00000221700.3:p.Gln3His
ENST00000011989.11:c.9G>T	ENSP00000011989.8:p.Gln3His
ENST00000221700.10:c.9G>T	ENSP00000221700.3:p.Gln3His
ENST00000392846.7:n.49+423G>T
ENST00000586927.2:c.9G>T	ENSP00000465514.1:p.Gln3His
ENST00000587671.2:c.9G>T	ENSP00000467443.2:p.Gln3His
ENST00000608168.1:n.62G>T
NM_001082.4:c.9G>T	NP_001073.3:p.Gln3His
NM_001082.5:c.9G>T MANE Select	NP_001073.3:p.Gln3His