Canonical Allele Identifier: CA505828253
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651459G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540648G>C , CM000681.2:g.15540648G>C GRCh38
NC_000019.9:g.15651459G>C , CM000681.1:g.15651459G>C GRCh37
NC_000019.8:g.15512459G>C NCBI36
NG_007987.1:g.37124G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.870G>C MANE Select ENSP00000269703.1:p.Gly290=
ENST00000269703.7:c.870G>C ENSP00000269703.1:p.Gly290=
ENST00000601005.2:c.870G>C ENSP00000469866.1:p.Gly290=
NM_173483.3:c.870G>C NP_775754.2:p.Gly290=
XM_011527692.1:c.870G>C XP_011525994.1:p.Gly290=
XM_011527693.1:c.870G>C XP_011525995.1:p.Gly290=
XM_011527692.2:c.870G>C XP_011525994.1:p.Gly290=
XM_011527693.2:c.870G>C XP_011525995.1:p.Gly290=
NM_173483.4:c.870G>C MANE Select NP_775754.2:p.Gly290=
Search 100 bp 5'
Search 100 bp 3'