Canonical Allele Identifier: CA505828262

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971448663
• gnomAD v4: 19-15540663-T-G
• MyVariant Identifiers: chr19:g.15651474T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540663T>G , CM000681.2:g.15540663T>G	GRCh38
NC_000019.9:g.15651474T>G , CM000681.1:g.15651474T>G	GRCh37
NC_000019.8:g.15512474T>G	NCBI36
NG_007987.1:g.37139T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.885T>G MANE Select	ENSP00000269703.1:p.Leu295=
ENST00000269703.7:c.885T>G	ENSP00000269703.1:p.Leu295=
ENST00000601005.2:c.885T>G	ENSP00000469866.1:p.Leu295=
NM_173483.3:c.885T>G	NP_775754.2:p.Leu295=
XM_011527692.1:c.885T>G	XP_011525994.1:p.Leu295=
XM_011527693.1:c.885T>G	XP_011525995.1:p.Leu295=
XM_011527692.2:c.885T>G	XP_011525994.1:p.Leu295=
XM_011527693.2:c.885T>G	XP_011525995.1:p.Leu295=
NM_173483.4:c.885T>G MANE Select	NP_775754.2:p.Leu295=