Canonical Allele Identifier: CA305829608

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1036540929
• MyVariant Identifiers: chr19:g.15654892C>T (hg19) ; chr19:g.15544081C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15544081C>T , CM000681.2:g.15544081C>T	GRCh38
NC_000019.9:g.15654892C>T , CM000681.1:g.15654892C>T	GRCh37
NC_000019.8:g.15515892C>T	NCBI36
NG_007987.1:g.40557C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269703.8:c.1006+44C>T MANE Select	ENSP00000269703.1:n.1006+44C>T
ENST00000269703.7:c.1006+44C>T	ENSP00000269703.1:n.1006+44C>T
ENST00000601005.2:c.1006+44C>T	ENSP00000469866.1:n.1006+44C>T
NM_173483.3:c.1006+44C>T	NP_775754.2:n.1006+44C>T
XM_011527692.1:c.1006+44C>T	XP_011525994.1:n.1006+44C>T
XM_011527693.1:c.1006+44C>T	XP_011525995.1:n.1006+44C>T
XM_011527692.2:c.1006+44C>T	XP_011525994.1:n.1006+44C>T
XM_011527693.2:c.1006+44C>T	XP_011525995.1:n.1006+44C>T
NM_173483.4:c.1006+44C>T MANE Select	NP_775754.2:n.1006+44C>T