Canonical Allele Identifier: CA404536422

Gene: CYP4F22

Linked Data

• MyVariant Identifiers: chr19:g.15651517C>G (hg19) ; chr19:g.15540706C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540706C>G , CM000681.2:g.15540706C>G	GRCh38
NC_000019.9:g.15651517C>G , CM000681.1:g.15651517C>G	GRCh37
NC_000019.8:g.15512517C>G	NCBI36
NG_007987.1:g.37182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.928C>G MANE Select	ENSP00000269703.1:p.Leu310Val
ENST00000269703.7:c.928C>G	ENSP00000269703.1:p.Leu310Val
ENST00000601005.2:c.928C>G	ENSP00000469866.1:p.Leu310Val
NM_173483.3:c.928C>G	NP_775754.2:p.Leu310Val
XM_011527692.1:c.928C>G	XP_011525994.1:p.Leu310Val
XM_011527693.1:c.928C>G	XP_011525995.1:p.Leu310Val
XM_011527692.2:c.928C>G	XP_011525994.1:p.Leu310Val
XM_011527693.2:c.928C>G	XP_011525995.1:p.Leu310Val
NM_173483.4:c.928C>G MANE Select	NP_775754.2:p.Leu310Val