Canonical Allele Identifier: CA9269719
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs146265982
ExAC: 19:15651449 G / A
gnomAD v2: 19-15651449-G-A
gnomAD v3: 19-15540638-G-A
gnomAD v4: 19-15540638-G-A
COSMIC: COSM3403864
MyVariant Identifiers: chr19:g.15651449G>A (hg19) chr19:g.15540638G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540638G>A , CM000681.2:g.15540638G>A GRCh38
NC_000019.9:g.15651449G>A , CM000681.1:g.15651449G>A GRCh37
NC_000019.8:g.15512449G>A NCBI36
NG_007987.1:g.37114G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.860G>A MANE Select ENSP00000269703.1:p.Arg287His
ENST00000269703.7:c.860G>A ENSP00000269703.1:p.Arg287His
ENST00000601005.2:c.860G>A ENSP00000469866.1:p.Arg287His
NM_173483.3:c.860G>A NP_775754.2:p.Arg287His
XM_011527692.1:c.860G>A XP_011525994.1:p.Arg287His
XM_011527693.1:c.860G>A XP_011525995.1:p.Arg287His
XM_011527692.2:c.860G>A XP_011525994.1:p.Arg287His
XM_011527693.2:c.860G>A XP_011525995.1:p.Arg287His
NM_173483.4:c.860G>A MANE Select NP_775754.2:p.Arg287His
Search 100 bp 5'
Search 100 bp 3'