Canonical Allele Identifier: CA2324927995
Gene: CYP4F22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540767G= , CM000681.2:g.15540767G= GRCh38
NC_000019.9:g.15651578G= , CM000681.1:g.15651578G= GRCh37
NC_000019.8:g.15512578G= NCBI36
NG_007987.1:g.37243G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+50G= MANE Select ENSP00000269703.1:n.939+50G=
ENST00000269703.7:c.939+50G= ENSP00000269703.1:n.939+50G=
ENST00000601005.2:c.939+50G= ENSP00000469866.1:n.939+50G=
NM_173483.3:c.939+50G= NP_775754.2:n.939+50G=
XM_011527692.1:c.939+50G= XP_011525994.1:n.939+50G=
XM_011527693.1:c.939+50G= XP_011525995.1:n.939+50G=
XM_011527692.2:c.939+50G= XP_011525994.1:n.939+50G=
XM_011527693.2:c.939+50G= XP_011525995.1:n.939+50G=
NM_173483.4:c.939+50G= MANE Select NP_775754.2:n.939+50G=