Canonical Allele Identifier: CA919111528
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs2234688

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158743_68158744insTGG , CM000674.2:g.68158743_68158744insTGG GRCh38
NC_000012.11:g.68552523_68552524insTGG , CM000674.1:g.68552523_68552524insTGG GRCh37
NC_000012.10:g.66838790_66838791insTGG NCBI36
NG_015840.1:g.5999_6000insCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-484_115-483insCAC MANE Select ENSP00000229135.3:n.115-484_115-483insCAC...
ENST00000229135.3:c.115-484_115-483insCAC ENSP00000229135.3:n.115-484_115-483insCAC...
NM_000619.2:c.115-484_115-483insCAC NP_000610.2:n.115-484_115-483insCAC
NM_000619.3:c.115-484_115-483insCAC MANE Select NP_000610.2:n.115-484_115-483insCAC