Canonical Allele Identifier: CA404536164

Gene: CYP4F22

Linked Data

• dbSNP Id: rs777093774
• MyVariant Identifiers: chr19:g.15651465G>C (hg19) ; chr19:g.15540654G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540654G>C , CM000681.2:g.15540654G>C	GRCh38
NC_000019.9:g.15651465G>C , CM000681.1:g.15651465G>C	GRCh37
NC_000019.8:g.15512465G>C	NCBI36
NG_007987.1:g.37130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.876G>C MANE Select	ENSP00000269703.1:p.Glu292Asp
ENST00000269703.7:c.876G>C	ENSP00000269703.1:p.Glu292Asp
ENST00000601005.2:c.876G>C	ENSP00000469866.1:p.Glu292Asp
NM_173483.3:c.876G>C	NP_775754.2:p.Glu292Asp
XM_011527692.1:c.876G>C	XP_011525994.1:p.Glu292Asp
XM_011527693.1:c.876G>C	XP_011525995.1:p.Glu292Asp
XM_011527692.2:c.876G>C	XP_011525994.1:p.Glu292Asp
XM_011527693.2:c.876G>C	XP_011525995.1:p.Glu292Asp
NM_173483.4:c.876G>C MANE Select	NP_775754.2:p.Glu292Asp