Canonical Allele Identifier: CA505828246
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15540636-G-C
MyVariant Identifiers: chr19:g.15651447G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540636G>C , CM000681.2:g.15540636G>C GRCh38
NC_000019.9:g.15651447G>C , CM000681.1:g.15651447G>C GRCh37
NC_000019.8:g.15512447G>C NCBI36
NG_007987.1:g.37112G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.858G>C MANE Select ENSP00000269703.1:p.Leu286=
ENST00000269703.7:c.858G>C ENSP00000269703.1:p.Leu286=
ENST00000601005.2:c.858G>C ENSP00000469866.1:p.Leu286=
NM_173483.3:c.858G>C NP_775754.2:p.Leu286=
XM_011527692.1:c.858G>C XP_011525994.1:p.Leu286=
XM_011527693.1:c.858G>C XP_011525995.1:p.Leu286=
XM_011527692.2:c.858G>C XP_011525994.1:p.Leu286=
XM_011527693.2:c.858G>C XP_011525995.1:p.Leu286=
NM_173483.4:c.858G>C MANE Select NP_775754.2:p.Leu286=
Search 100 bp 5'
Search 100 bp 3'