Canonical Allele Identifier: CA404535991

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540613-A-G
• MyVariant Identifiers: chr19:g.15651424A>G (hg19) ; chr19:g.15540613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540613A>G , CM000681.2:g.15540613A>G	GRCh38
NC_000019.9:g.15651424A>G , CM000681.1:g.15651424A>G	GRCh37
NC_000019.8:g.15512424A>G	NCBI36
NG_007987.1:g.37089A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.835A>G MANE Select	ENSP00000269703.1:p.Ile279Val
ENST00000269703.7:c.835A>G	ENSP00000269703.1:p.Ile279Val
ENST00000601005.2:c.835A>G	ENSP00000469866.1:p.Ile279Val
NM_173483.3:c.835A>G	NP_775754.2:p.Ile279Val
XM_011527692.1:c.835A>G	XP_011525994.1:p.Ile279Val
XM_011527693.1:c.835A>G	XP_011525995.1:p.Ile279Val
XM_011527692.2:c.835A>G	XP_011525994.1:p.Ile279Val
XM_011527693.2:c.835A>G	XP_011525995.1:p.Ile279Val
NM_173483.4:c.835A>G MANE Select	NP_775754.2:p.Ile279Val