Canonical Allele Identifier: CA505828279
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15540699-T-C
MyVariant Identifiers: chr19:g.15651510T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540699T>C , CM000681.2:g.15540699T>C GRCh38
NC_000019.9:g.15651510T>C , CM000681.1:g.15651510T>C GRCh37
NC_000019.8:g.15512510T>C NCBI36
NG_007987.1:g.37175T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.921T>C MANE Select ENSP00000269703.1:p.Asp307=
ENST00000269703.7:c.921T>C ENSP00000269703.1:p.Asp307=
ENST00000601005.2:c.921T>C ENSP00000469866.1:p.Asp307=
NM_173483.3:c.921T>C NP_775754.2:p.Asp307=
XM_011527692.1:c.921T>C XP_011525994.1:p.Asp307=
XM_011527693.1:c.921T>C XP_011525995.1:p.Asp307=
XM_011527692.2:c.921T>C XP_011525994.1:p.Asp307=
XM_011527693.2:c.921T>C XP_011525995.1:p.Asp307=
NM_173483.4:c.921T>C MANE Select NP_775754.2:p.Asp307=
Search 100 bp 5'
Search 100 bp 3'