Canonical Allele Identifier: CA505828249
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651450T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540639T>C , CM000681.2:g.15540639T>C GRCh38
NC_000019.9:g.15651450T>C , CM000681.1:g.15651450T>C GRCh37
NC_000019.8:g.15512450T>C NCBI36
NG_007987.1:g.37115T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.861T>C MANE Select ENSP00000269703.1:p.Arg287=
ENST00000269703.7:c.861T>C ENSP00000269703.1:p.Arg287=
ENST00000601005.2:c.861T>C ENSP00000469866.1:p.Arg287=
NM_173483.3:c.861T>C NP_775754.2:p.Arg287=
XM_011527692.1:c.861T>C XP_011525994.1:p.Arg287=
XM_011527693.1:c.861T>C XP_011525995.1:p.Arg287=
XM_011527692.2:c.861T>C XP_011525994.1:p.Arg287=
XM_011527693.2:c.861T>C XP_011525995.1:p.Arg287=
NM_173483.4:c.861T>C MANE Select NP_775754.2:p.Arg287=