Canonical Allele Identifier: CA404536059
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540629G>C , CM000681.2:g.15540629G>C GRCh38
NC_000019.9:g.15651440G>C , CM000681.1:g.15651440G>C GRCh37
NC_000019.8:g.15512440G>C NCBI36
NG_007987.1:g.37105G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.851G>C MANE Select ENSP00000269703.1:p.Arg284Pro
ENST00000269703.7:c.851G>C ENSP00000269703.1:p.Arg284Pro
ENST00000601005.2:c.851G>C ENSP00000469866.1:p.Arg284Pro
NM_173483.3:c.851G>C NP_775754.2:p.Arg284Pro
XM_011527692.1:c.851G>C XP_011525994.1:p.Arg284Pro
XM_011527693.1:c.851G>C XP_011525995.1:p.Arg284Pro
XM_011527692.2:c.851G>C XP_011525994.1:p.Arg284Pro
XM_011527693.2:c.851G>C XP_011525995.1:p.Arg284Pro
NM_173483.4:c.851G>C MANE Select NP_775754.2:p.Arg284Pro