Canonical Allele Identifier: CA404526672
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529719A>C , CM000681.2:g.15529719A>C GRCh38
NC_000019.9:g.15640530A>C , CM000681.1:g.15640530A>C GRCh37
NC_000019.8:g.15501530A>C NCBI36
NG_007987.1:g.26195A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.233A>C MANE Select ENSP00000269703.1:p.Asn78Thr
ENST00000269703.7:c.233A>C ENSP00000269703.1:p.Asn78Thr
ENST00000601005.2:c.233A>C ENSP00000469866.1:p.Asn78Thr
NM_173483.3:c.233A>C NP_775754.2:p.Asn78Thr
XM_011527692.1:c.233A>C XP_011525994.1:p.Asn78Thr
XM_011527693.1:c.233A>C XP_011525995.1:p.Asn78Thr
XM_011527692.2:c.233A>C XP_011525994.1:p.Asn78Thr
XM_011527693.2:c.233A>C XP_011525995.1:p.Asn78Thr
NM_173483.4:c.233A>C MANE Select NP_775754.2:p.Asn78Thr