Canonical Allele Identifier: CA505828243
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651444A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540633A>T , CM000681.2:g.15540633A>T GRCh38
NC_000019.9:g.15651444A>T , CM000681.1:g.15651444A>T GRCh37
NC_000019.8:g.15512444A>T NCBI36
NG_007987.1:g.37109A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.855A>T MANE Select ENSP00000269703.1:p.Ala285=
ENST00000269703.7:c.855A>T ENSP00000269703.1:p.Ala285=
ENST00000601005.2:c.855A>T ENSP00000469866.1:p.Ala285=
NM_173483.3:c.855A>T NP_775754.2:p.Ala285=
XM_011527692.1:c.855A>T XP_011525994.1:p.Ala285=
XM_011527693.1:c.855A>T XP_011525995.1:p.Ala285=
XM_011527692.2:c.855A>T XP_011525994.1:p.Ala285=
XM_011527693.2:c.855A>T XP_011525995.1:p.Ala285=
NM_173483.4:c.855A>T MANE Select NP_775754.2:p.Ala285=