Canonical Allele Identifier: CA1838717726
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140726A= , CM000671.2:g.21140726A= GRCh38
NC_000009.11:g.21140725A= , CM000671.1:g.21140725A= GRCh37
NC_000009.10:g.21130725A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*257T= MANE Select ENSP00000369578.2:n.*257T=
ENST00000380229.3:c.*257T= ENSP00000369578.2:n.*257T=
NM_002177.1:c.*257T= NP_002168.1:n.*257T=
NM_002177.2:c.*257T= NP_002168.1:n.*257T=
NM_002177.3:c.*257T= MANE Select NP_002168.1:n.*257T=