Canonical Allele Identifier: CA404535999
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540614T>G , CM000681.2:g.15540614T>G GRCh38
NC_000019.9:g.15651425T>G , CM000681.1:g.15651425T>G GRCh37
NC_000019.8:g.15512425T>G NCBI36
NG_007987.1:g.37090T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.836T>G MANE Select ENSP00000269703.1:p.Ile279Ser
ENST00000269703.7:c.836T>G ENSP00000269703.1:p.Ile279Ser
ENST00000601005.2:c.836T>G ENSP00000469866.1:p.Ile279Ser
NM_173483.3:c.836T>G NP_775754.2:p.Ile279Ser
XM_011527692.1:c.836T>G XP_011525994.1:p.Ile279Ser
XM_011527693.1:c.836T>G XP_011525995.1:p.Ile279Ser
XM_011527692.2:c.836T>G XP_011525994.1:p.Ile279Ser
XM_011527693.2:c.836T>G XP_011525995.1:p.Ile279Ser
NM_173483.4:c.836T>G MANE Select NP_775754.2:p.Ile279Ser