Canonical Allele Identifier: CA919111519
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1555186217

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158740_68158742del , CM000674.2:g.68158740_68158742del GRCh38
NC_000012.11:g.68552520_68552522del , CM000674.1:g.68552520_68552522del GRCh37
NC_000012.10:g.66838787_66838789del NCBI36
NG_015840.1:g.6000_6002del

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-483_115-481del MANE Select ENSP00000229135.3:n.115-483_115-481del
ENST00000229135.3:c.115-483_115-481del ENSP00000229135.3:n.115-483_115-481del
NM_000619.2:c.115-483_115-481del NP_000610.2:n.115-483_115-481del
NM_000619.3:c.115-483_115-481del MANE Select NP_000610.2:n.115-483_115-481del