Canonical Allele Identifier: CA305826490
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 560312
ClinVar RCV Id: RCV000678403
dbSNP Id: rs370734976
gnomAD v2: 19-15651506-T-C
gnomAD v4: 19-15540695-T-C
MyVariant Identifiers: chr19:g.15651506T>C (hg19) chr19:g.15540695T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540695T>C , CM000681.2:g.15540695T>C GRCh38
NC_000019.9:g.15651506T>C , CM000681.1:g.15651506T>C GRCh37
NC_000019.8:g.15512506T>C NCBI36
NG_007987.1:g.37171T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.917T>C MANE Select ENSP00000269703.1:p.Ile306Thr
ENST00000269703.7:c.917T>C ENSP00000269703.1:p.Ile306Thr
ENST00000601005.2:c.917T>C ENSP00000469866.1:p.Ile306Thr
NM_173483.3:c.917T>C NP_775754.2:p.Ile306Thr
XM_011527692.1:c.917T>C XP_011525994.1:p.Ile306Thr
XM_011527693.1:c.917T>C XP_011525995.1:p.Ile306Thr
XM_011527692.2:c.917T>C XP_011525994.1:p.Ile306Thr
XM_011527693.2:c.917T>C XP_011525995.1:p.Ile306Thr
NM_173483.4:c.917T>C MANE Select NP_775754.2:p.Ile306Thr
Search 100 bp 5'
Search 100 bp 3'