Canonical Allele Identifier: CA2324923158
Gene: CYP4F22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529706C= , CM000681.2:g.15529706C= GRCh38
NC_000019.9:g.15640517C= , CM000681.1:g.15640517C= GRCh37
NC_000019.8:g.15501517C= NCBI36
NG_007987.1:g.26182C=

Transcript Alleles

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