Canonical Allele Identifier: CA404579864

Gene: CYP4F2

Linked Data

• MyVariant Identifiers: chr19:g.16008305G>T (hg19) ; chr19:g.15897495G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897495G>T , CM000681.2:g.15897495G>T	GRCh38
NC_000019.9:g.16008305G>T , CM000681.1:g.16008305G>T	GRCh37
NC_000019.8:g.15869305G>T	NCBI36
NG_007971.2:g.5580C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.117C>A MANE Select	ENSP00000221700.3:p.Tyr39Ter
ENST00000011989.11:c.117C>A	ENSP00000011989.8:p.Tyr39Ter
ENST00000221700.10:c.117C>A	ENSP00000221700.3:p.Tyr39Ter
ENST00000392846.7:n.49+531C>A
ENST00000586927.2:c.117C>A	ENSP00000465514.1:p.Tyr39Ter
ENST00000587671.2:c.117C>A	ENSP00000467443.2:p.Tyr39Ter
ENST00000608168.1:n.170C>A
NM_001082.4:c.117C>A	NP_001073.3:p.Tyr39Ter
NM_001082.5:c.117C>A MANE Select	NP_001073.3:p.Tyr39Ter