Canonical Allele Identifier: CA13122384
Gene: IFNW1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10964859

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140673C>G , CM000671.2:g.21140673C>G GRCh38
NC_000009.11:g.21140672C>G , CM000671.1:g.21140672C>G GRCh37
NC_000009.10:g.21130672C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002177.1:c.*310G>C VV NP_002168.1:p.=
NM_002177.2:c.*310G>C VV NP_002168.1:p.=
ENST00000380229.3:c.*310G>C ENSP00000369578.2:p.=