Canonical Allele Identifier: CA9269772
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1222926
ClinVar RCV Id: RCV001599104
dbSNP Id: rs55832992
ExAC: 19:15651568 C / A
gnomAD v2: 19-15651568-C-A
gnomAD v3: 19-15540757-C-A
gnomAD v4: 19-15540757-C-A
MyVariant Identifiers: chr19:g.15651568C>A (hg19) chr19:g.15540757C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540757C>A , CM000681.2:g.15540757C>A GRCh38
NC_000019.9:g.15651568C>A , CM000681.1:g.15651568C>A GRCh37
NC_000019.8:g.15512568C>A NCBI36
NG_007987.1:g.37233C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+40C>A MANE Select ENSP00000269703.1:n.939+40C>A
ENST00000269703.7:c.939+40C>A ENSP00000269703.1:n.939+40C>A
ENST00000601005.2:c.939+40C>A ENSP00000469866.1:n.939+40C>A
NM_173483.3:c.939+40C>A NP_775754.2:n.939+40C>A
XM_011527692.1:c.939+40C>A XP_011525994.1:n.939+40C>A
XM_011527693.1:c.939+40C>A XP_011525995.1:n.939+40C>A
XM_011527692.2:c.939+40C>A XP_011525994.1:n.939+40C>A
XM_011527693.2:c.939+40C>A XP_011525995.1:n.939+40C>A
NM_173483.4:c.939+40C>A MANE Select NP_775754.2:n.939+40C>A
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