Canonical Allele Identifier: CA2324927840
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs1971442760
gnomAD v4: 19-15540352-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540352A>G , CM000681.2:g.15540352A>G GRCh38
NC_000019.9:g.15651163A>G , CM000681.1:g.15651163A>G GRCh37
NC_000019.8:g.15512163A>G NCBI36
NG_007987.1:g.36828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.672-98A>G MANE Select ENSP00000269703.1:n.672-98A>G
ENST00000269703.7:c.672-98A>G ENSP00000269703.1:n.672-98A>G
ENST00000601005.2:c.672-98A>G ENSP00000469866.1:n.672-98A>G
NM_173483.3:c.672-98A>G NP_775754.2:n.672-98A>G
XM_011527692.1:c.672-98A>G XP_011525994.1:n.672-98A>G
XM_011527693.1:c.672-98A>G XP_011525995.1:n.672-98A>G
XM_011527692.2:c.672-98A>G XP_011525994.1:n.672-98A>G
XM_011527693.2:c.672-98A>G XP_011525995.1:n.672-98A>G
NM_173483.4:c.672-98A>G MANE Select NP_775754.2:n.672-98A>G
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