Canonical Allele Identifier: CA404535332
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651266T>C (hg19) chr19:g.15540455T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540455T>C , CM000681.2:g.15540455T>C GRCh38
NC_000019.9:g.15651266T>C , CM000681.1:g.15651266T>C GRCh37
NC_000019.8:g.15512266T>C NCBI36
NG_007987.1:g.36931T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.677T>C MANE Select ENSP00000269703.1:p.Met226Thr
ENST00000269703.7:c.677T>C ENSP00000269703.1:p.Met226Thr
ENST00000601005.2:c.677T>C ENSP00000469866.1:p.Met226Thr
NM_173483.3:c.677T>C NP_775754.2:p.Met226Thr
XM_011527692.1:c.677T>C XP_011525994.1:p.Met226Thr
XM_011527693.1:c.677T>C XP_011525995.1:p.Met226Thr
XM_011527692.2:c.677T>C XP_011525994.1:p.Met226Thr
XM_011527693.2:c.677T>C XP_011525995.1:p.Met226Thr
NM_173483.4:c.677T>C MANE Select NP_775754.2:p.Met226Thr
Search 100 bp 5'
Search 100 bp 3'