Canonical Allele Identifier: CA505872464

Gene: CYP4F2

Linked Data

• dbSNP Id: rs2145017547
• MyVariant Identifiers: chr19:g.16008233G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897423G>A , CM000681.2:g.15897423G>A	GRCh38
NC_000019.9:g.16008233G>A , CM000681.1:g.16008233G>A	GRCh37
NC_000019.8:g.15869233G>A	NCBI36
NG_007971.2:g.5652C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.189C>T MANE Select	ENSP00000221700.3:p.His63=
ENST00000011989.11:c.189C>T	ENSP00000011989.8:p.His63=
ENST00000221700.10:c.189C>T	ENSP00000221700.3:p.His63=
ENST00000392846.7:n.49+603C>T
ENST00000586927.2:c.189C>T	ENSP00000465514.1:p.His63=
ENST00000587671.2:c.189C>T	ENSP00000467443.2:p.His63=
ENST00000608168.1:n.242C>T
NM_001082.4:c.189C>T	NP_001073.3:p.His63=
NM_001082.5:c.189C>T MANE Select	NP_001073.3:p.His63=