Canonical Allele Identifier: CA404536016
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs1971447263

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540617A>C , CM000681.2:g.15540617A>C GRCh38
NC_000019.9:g.15651428A>C , CM000681.1:g.15651428A>C GRCh37
NC_000019.8:g.15512428A>C NCBI36
NG_007987.1:g.37093A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.839A>C MANE Select ENSP00000269703.1:p.Gln280Pro
ENST00000269703.7:c.839A>C ENSP00000269703.1:p.Gln280Pro
ENST00000601005.2:c.839A>C ENSP00000469866.1:p.Gln280Pro
NM_173483.3:c.839A>C NP_775754.2:p.Gln280Pro
XM_011527692.1:c.839A>C XP_011525994.1:p.Gln280Pro
XM_011527693.1:c.839A>C XP_011525995.1:p.Gln280Pro
XM_011527692.2:c.839A>C XP_011525994.1:p.Gln280Pro
XM_011527693.2:c.839A>C XP_011525995.1:p.Gln280Pro
NM_173483.4:c.839A>C MANE Select NP_775754.2:p.Gln280Pro