Canonical Allele Identifier: CA2324929581

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971494849

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15544091A>G , CM000681.2:g.15544091A>G	GRCh38
NC_000019.9:g.15654902A>G , CM000681.1:g.15654902A>G	GRCh37
NC_000019.8:g.15515902A>G	NCBI36
NG_007987.1:g.40567A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269703.8:c.1006+54A>G MANE Select	ENSP00000269703.1:n.1006+54A>G
ENST00000269703.7:c.1006+54A>G	ENSP00000269703.1:n.1006+54A>G
ENST00000601005.2:c.1006+54A>G	ENSP00000469866.1:n.1006+54A>G
NM_173483.3:c.1006+54A>G	NP_775754.2:n.1006+54A>G
XM_011527692.1:c.1006+54A>G	XP_011525994.1:n.1006+54A>G
XM_011527693.1:c.1006+54A>G	XP_011525995.1:n.1006+54A>G
XM_011527692.2:c.1006+54A>G	XP_011525994.1:n.1006+54A>G
XM_011527693.2:c.1006+54A>G	XP_011525995.1:n.1006+54A>G
NM_173483.4:c.1006+54A>G MANE Select	NP_775754.2:n.1006+54A>G