Canonical Allele Identifier: CA2324927991
Gene: CYP4F22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540763T= , CM000681.2:g.15540763T= GRCh38
NC_000019.9:g.15651574T= , CM000681.1:g.15651574T= GRCh37
NC_000019.8:g.15512574T= NCBI36
NG_007987.1:g.37239T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+46T= MANE Select ENSP00000269703.1:n.939+46T=
ENST00000269703.7:c.939+46T= ENSP00000269703.1:n.939+46T=
ENST00000601005.2:c.939+46T= ENSP00000469866.1:n.939+46T=
NM_173483.3:c.939+46T= NP_775754.2:n.939+46T=
XM_011527692.1:c.939+46T= XP_011525994.1:n.939+46T=
XM_011527693.1:c.939+46T= XP_011525995.1:n.939+46T=
XM_011527692.2:c.939+46T= XP_011525994.1:n.939+46T=
XM_011527693.2:c.939+46T= XP_011525995.1:n.939+46T=
NM_173483.4:c.939+46T= MANE Select NP_775754.2:n.939+46T=