Canonical Allele Identifier: CA404536462
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651527G>C (hg19) chr19:g.15540716G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540716G>C , CM000681.2:g.15540716G>C GRCh38
NC_000019.9:g.15651527G>C , CM000681.1:g.15651527G>C GRCh37
NC_000019.8:g.15512527G>C NCBI36
NG_007987.1:g.37192G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.938G>C MANE Select ENSP00000269703.1:p.Arg313Thr
ENST00000269703.7:c.938G>C ENSP00000269703.1:p.Arg313Thr
ENST00000601005.2:c.938G>C ENSP00000469866.1:p.Arg313Thr
NM_173483.3:c.938G>C NP_775754.2:p.Arg313Thr
XM_011527692.1:c.938G>C XP_011525994.1:p.Arg313Thr
XM_011527693.1:c.938G>C XP_011525995.1:p.Arg313Thr
XM_011527692.2:c.938G>C XP_011525994.1:p.Arg313Thr
XM_011527693.2:c.938G>C XP_011525995.1:p.Arg313Thr
NM_173483.4:c.938G>C MANE Select NP_775754.2:p.Arg313Thr
Search 100 bp 5'
Search 100 bp 3'