Canonical Allele Identifier: CA2324927939
Gene: CYP4F22 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540737A= , CM000681.2:g.15540737A= GRCh38
NC_000019.9:g.15651548A= , CM000681.1:g.15651548A= GRCh37
NC_000019.8:g.15512548A= NCBI36
NG_007987.1:g.37213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+20A= MANE Select ENSP00000269703.1:n.939+20A=
ENST00000269703.7:c.939+20A= ENSP00000269703.1:n.939+20A=
ENST00000601005.2:c.939+20A= ENSP00000469866.1:n.939+20A=
NM_173483.3:c.939+20A= NP_775754.2:n.939+20A=
XM_011527692.1:c.939+20A= XP_011525994.1:n.939+20A=
XM_011527693.1:c.939+20A= XP_011525995.1:n.939+20A=
XM_011527692.2:c.939+20A= XP_011525994.1:n.939+20A=
XM_011527693.2:c.939+20A= XP_011525995.1:n.939+20A=
NM_173483.4:c.939+20A= MANE Select NP_775754.2:n.939+20A=
Search 100 bp 5'
Search 100 bp 3'