Canonical Allele Identifier: CA9269720
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs146265982

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540638G>C , CM000681.2:g.15540638G>C GRCh38
NC_000019.9:g.15651449G>C , CM000681.1:g.15651449G>C GRCh37
NC_000019.8:g.15512449G>C NCBI36
NG_007987.1:g.37114G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.860G>C MANE Select ENSP00000269703.1:p.Arg287Pro
ENST00000269703.7:c.860G>C ENSP00000269703.1:p.Arg287Pro
ENST00000601005.2:c.860G>C ENSP00000469866.1:p.Arg287Pro
NM_173483.3:c.860G>C NP_775754.2:p.Arg287Pro
XM_011527692.1:c.860G>C XP_011525994.1:p.Arg287Pro
XM_011527693.1:c.860G>C XP_011525995.1:p.Arg287Pro
XM_011527692.2:c.860G>C XP_011525994.1:p.Arg287Pro
XM_011527693.2:c.860G>C XP_011525995.1:p.Arg287Pro
NM_173483.4:c.860G>C MANE Select NP_775754.2:p.Arg287Pro