Canonical Allele Identifier: CA505828163

Gene: CYP4F22

Linked Data

• MyVariant Identifiers: chr19:g.15651315G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540504G>C , CM000681.2:g.15540504G>C	GRCh38
NC_000019.9:g.15651315G>C , CM000681.1:g.15651315G>C	GRCh37
NC_000019.8:g.15512315G>C	NCBI36
NG_007987.1:g.36980G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.726G>C MANE Select	ENSP00000269703.1:p.Arg242=
ENST00000269703.7:c.726G>C	ENSP00000269703.1:p.Arg242=
ENST00000601005.2:c.726G>C	ENSP00000469866.1:p.Arg242=
NM_173483.3:c.726G>C	NP_775754.2:p.Arg242=
XM_011527692.1:c.726G>C	XP_011525994.1:p.Arg242=
XM_011527693.1:c.726G>C	XP_011525995.1:p.Arg242=
XM_011527692.2:c.726G>C	XP_011525994.1:p.Arg242=
XM_011527693.2:c.726G>C	XP_011525995.1:p.Arg242=
NM_173483.4:c.726G>C MANE Select	NP_775754.2:p.Arg242=