Canonical Allele Identifier: CA505828240
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651441G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540630G>T , CM000681.2:g.15540630G>T GRCh38
NC_000019.9:g.15651441G>T , CM000681.1:g.15651441G>T GRCh37
NC_000019.8:g.15512441G>T NCBI36
NG_007987.1:g.37106G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.852G>T MANE Select ENSP00000269703.1:p.Arg284=
ENST00000269703.7:c.852G>T ENSP00000269703.1:p.Arg284=
ENST00000601005.2:c.852G>T ENSP00000469866.1:p.Arg284=
NM_173483.3:c.852G>T NP_775754.2:p.Arg284=
XM_011527692.1:c.852G>T XP_011525994.1:p.Arg284=
XM_011527693.1:c.852G>T XP_011525995.1:p.Arg284=
XM_011527692.2:c.852G>T XP_011525994.1:p.Arg284=
XM_011527693.2:c.852G>T XP_011525995.1:p.Arg284=
NM_173483.4:c.852G>T MANE Select NP_775754.2:p.Arg284=