Canonical Allele Identifier: CA2324927881
Gene: CYP4F22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540441C= , CM000681.2:g.15540441C= GRCh38
NC_000019.9:g.15651252C= , CM000681.1:g.15651252C= GRCh37
NC_000019.8:g.15512252C= NCBI36
NG_007987.1:g.36917C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.672-9C= MANE Select ENSP00000269703.1:n.672-9C=
ENST00000269703.7:c.672-9C= ENSP00000269703.1:n.672-9C=
ENST00000601005.2:c.672-9C= ENSP00000469866.1:n.672-9C=
NM_173483.3:c.672-9C= NP_775754.2:n.672-9C=
XM_011527692.1:c.672-9C= XP_011525994.1:n.672-9C=
XM_011527693.1:c.672-9C= XP_011525995.1:n.672-9C=
XM_011527692.2:c.672-9C= XP_011525994.1:n.672-9C=
XM_011527693.2:c.672-9C= XP_011525995.1:n.672-9C=
NM_173483.4:c.672-9C= MANE Select NP_775754.2:n.672-9C=
Search 100 bp 5'
Search 100 bp 3'