Canonical Allele Identifier: CA2642410969

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971319893
• gnomAD v4: 19-15529637-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15529637G>T , CM000681.2:g.15529637G>T	GRCh38
NC_000019.9:g.15640448G>T , CM000681.1:g.15640448G>T	GRCh37
NC_000019.8:g.15501448G>T	NCBI36
NG_007987.1:g.26113G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.223-72G>T MANE Select	ENSP00000269703.1:n.223-72G>T
ENST00000269703.7:c.223-72G>T	ENSP00000269703.1:n.223-72G>T
ENST00000601005.2:c.223-72G>T	ENSP00000469866.1:n.223-72G>T
NM_173483.3:c.223-72G>T	NP_775754.2:n.223-72G>T
XM_011527692.1:c.223-72G>T	XP_011525994.1:n.223-72G>T
XM_011527693.1:c.223-72G>T	XP_011525995.1:n.223-72G>T
XM_011527692.2:c.223-72G>T	XP_011525994.1:n.223-72G>T
XM_011527693.2:c.223-72G>T	XP_011525995.1:n.223-72G>T
NM_173483.4:c.223-72G>T MANE Select	NP_775754.2:n.223-72G>T