Canonical Allele Identifier: CA2324927962
Gene: CYP4F22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540745G= , CM000681.2:g.15540745G= GRCh38
NC_000019.9:g.15651556G= , CM000681.1:g.15651556G= GRCh37
NC_000019.8:g.15512556G= NCBI36
NG_007987.1:g.37221G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+28G= MANE Select ENSP00000269703.1:n.939+28G=
ENST00000269703.7:c.939+28G= ENSP00000269703.1:n.939+28G=
ENST00000601005.2:c.939+28G= ENSP00000469866.1:n.939+28G=
NM_173483.3:c.939+28G= NP_775754.2:n.939+28G=
XM_011527692.1:c.939+28G= XP_011525994.1:n.939+28G=
XM_011527693.1:c.939+28G= XP_011525995.1:n.939+28G=
XM_011527692.2:c.939+28G= XP_011525994.1:n.939+28G=
XM_011527693.2:c.939+28G= XP_011525995.1:n.939+28G=
NM_173483.4:c.939+28G= MANE Select NP_775754.2:n.939+28G=
Search 100 bp 5'
Search 100 bp 3'