Canonical Allele Identifier: CA505828175

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540525-C-T
• MyVariant Identifiers: chr19:g.15651336C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540525C>T , CM000681.2:g.15540525C>T	GRCh38
NC_000019.9:g.15651336C>T , CM000681.1:g.15651336C>T	GRCh37
NC_000019.8:g.15512336C>T	NCBI36
NG_007987.1:g.37001C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.747C>T MANE Select	ENSP00000269703.1:p.His249=
ENST00000269703.7:c.747C>T	ENSP00000269703.1:p.His249=
ENST00000601005.2:c.747C>T	ENSP00000469866.1:p.His249=
NM_173483.3:c.747C>T	NP_775754.2:p.His249=
XM_011527692.1:c.747C>T	XP_011525994.1:p.His249=
XM_011527693.1:c.747C>T	XP_011525995.1:p.His249=
XM_011527692.2:c.747C>T	XP_011525994.1:p.His249=
XM_011527693.2:c.747C>T	XP_011525995.1:p.His249=
NM_173483.4:c.747C>T MANE Select	NP_775754.2:p.His249=