Canonical Allele Identifier: CA16043077
Gene: CYP4F22 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372938
ClinVar RCV Id: RCV000414461
dbSNP Id: rs1057518087

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529699C>G , CM000681.2:g.15529699C>G GRCh38
NC_000019.8:g.15501510C>G NCBI36
NC_000019.9:g.15640510C>G , CM000681.1:g.15640510C>G GRCh37
NG_007987.1:g.26175C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.7:c.223-10C>G ENSP00000269703.1:p.=
ENST00000601005.2:c.223-10C>G ENSP00000469866.1:p.=
NM_173483.3:c.223-10C>G NP_775754.2:p.=
XM_011527692.1:c.223-10C>G XP_011525994.1:p.=
XM_011527693.1:c.223-10C>G XP_011525995.1:p.=