Canonical Allele Identifier: CA2324923128
Gene: CYP4F22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529659G= , CM000681.2:g.15529659G= GRCh38
NC_000019.9:g.15640470G= , CM000681.1:g.15640470G= GRCh37
NC_000019.8:g.15501470G= NCBI36
NG_007987.1:g.26135G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.223-50G= MANE Select ENSP00000269703.1:n.223-50G=
ENST00000269703.7:c.223-50G= ENSP00000269703.1:n.223-50G=
ENST00000601005.2:c.223-50G= ENSP00000469866.1:n.223-50G=
NM_173483.3:c.223-50G= NP_775754.2:n.223-50G=
XM_011527692.1:c.223-50G= XP_011525994.1:n.223-50G=
XM_011527693.1:c.223-50G= XP_011525995.1:n.223-50G=
XM_011527692.2:c.223-50G= XP_011525994.1:n.223-50G=
XM_011527693.2:c.223-50G= XP_011525995.1:n.223-50G=
NM_173483.4:c.223-50G= MANE Select NP_775754.2:n.223-50G=