Canonical Allele Identifier: CA505828258

Gene: CYP4F22

Linked Data

• MyVariant Identifiers: chr19:g.15651468C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540657C>G , CM000681.2:g.15540657C>G	GRCh38
NC_000019.9:g.15651468C>G , CM000681.1:g.15651468C>G	GRCh37
NC_000019.8:g.15512468C>G	NCBI36
NG_007987.1:g.37133C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.879C>G MANE Select	ENSP00000269703.1:p.Ala293=
ENST00000269703.7:c.879C>G	ENSP00000269703.1:p.Ala293=
ENST00000601005.2:c.879C>G	ENSP00000469866.1:p.Ala293=
NM_173483.3:c.879C>G	NP_775754.2:p.Ala293=
XM_011527692.1:c.879C>G	XP_011525994.1:p.Ala293=
XM_011527693.1:c.879C>G	XP_011525995.1:p.Ala293=
XM_011527692.2:c.879C>G	XP_011525994.1:p.Ala293=
XM_011527693.2:c.879C>G	XP_011525995.1:p.Ala293=
NM_173483.4:c.879C>G MANE Select	NP_775754.2:p.Ala293=