Canonical Allele Identifier: CA919111518
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1555186216

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158740_68158742delinsA , CM000674.2:g.68158740_68158742delinsA GRCh38
NC_000012.11:g.68552520_68552522delinsA , CM000674.1:g.68552520_68552522delinsA GRCh37
NC_000012.10:g.66838787_66838789delinsA NCBI36
NG_015840.1:g.6000_6002delinsT

Transcript Alleles

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