Canonical Allele Identifier: CA114616
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 909
dbSNP Id: rs118203935

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15549170C>T , CM000681.2:g.15549170C>T GRCh38
NC_000019.9:g.15659981C>T , CM000681.1:g.15659981C>T GRCh37
NC_000019.8:g.15520981C>T NCBI36
NG_007987.1:g.45646C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.1303C>T MANE Select ENSP00000269703.1:p.His435Tyr
ENST00000269703.7:c.1303C>T ENSP00000269703.1:p.His435Tyr
ENST00000601005.2:c.1303C>T ENSP00000469866.1:p.His435Tyr
NM_173483.3:c.1303C>T NP_775754.2:p.His435Tyr
XM_011527692.1:c.1303C>T XP_011525994.1:p.His435Tyr
XM_011527693.1:c.1303C>T XP_011525995.1:p.His435Tyr
XM_011527692.2:c.1303C>T XP_011525994.1:p.His435Tyr
XM_011527693.2:c.1303C>T XP_011525995.1:p.His435Tyr
NM_173483.4:c.1303C>T MANE Select NP_775754.2:p.His435Tyr