Canonical Allele Identifier: CA2043754722
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1882641321

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158742_68158748del , CM000674.2:g.68158742_68158748del GRCh38
NC_000012.11:g.68552522_68552528del , CM000674.1:g.68552522_68552528del GRCh37
NC_000012.10:g.66838789_66838795del NCBI36
NG_015840.1:g.5996_6002del

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-487_115-481del MANE Select ENSP00000229135.3:n.115-487_115-481del
ENST00000229135.3:c.115-487_115-481del ENSP00000229135.3:n.115-487_115-481del
NM_000619.2:c.115-487_115-481del NP_000610.2:n.115-487_115-481del
NM_000619.3:c.115-487_115-481del MANE Select NP_000610.2:n.115-487_115-481del