Canonical Allele Identifier: CA404536002
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540615C>G , CM000681.2:g.15540615C>G GRCh38
NC_000019.9:g.15651426C>G , CM000681.1:g.15651426C>G GRCh37
NC_000019.8:g.15512426C>G NCBI36
NG_007987.1:g.37091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.837C>G MANE Select ENSP00000269703.1:p.Ile279Met
ENST00000269703.7:c.837C>G ENSP00000269703.1:p.Ile279Met
ENST00000601005.2:c.837C>G ENSP00000469866.1:p.Ile279Met
NM_173483.3:c.837C>G NP_775754.2:p.Ile279Met
XM_011527692.1:c.837C>G XP_011525994.1:p.Ile279Met
XM_011527693.1:c.837C>G XP_011525995.1:p.Ile279Met
XM_011527692.2:c.837C>G XP_011525994.1:p.Ile279Met
XM_011527693.2:c.837C>G XP_011525995.1:p.Ile279Met
NM_173483.4:c.837C>G MANE Select NP_775754.2:p.Ile279Met