Canonical Allele Identifier: CA691232962
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs34079299
gnomAD v3: 12-68158714-A-AGTGTGTGTGT
gnomAD v4: 12-68158714-A-AGTGTGTGTGT
MyVariant Identifiers: chr12:g.68552494_68552495insGTGTGTGTGT (hg19) chr12:g.68158714_68158715insGTGTGTGTGT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158734_68158743dup , CM000674.2:g.68158734_68158743dup GRCh38
NC_000012.11:g.68552514_68552523dup , CM000674.1:g.68552514_68552523dup GRCh37
NC_000012.10:g.66838781_66838790dup NCBI36
NG_015840.1:g.6018_6027dup

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-465_115-456dup MANE Select ENSP00000229135.3:n.115-465_115-456dup
ENST00000229135.3:c.115-465_115-456dup ENSP00000229135.3:n.115-465_115-456dup
NM_000619.2:c.115-465_115-456dup NP_000610.2:n.115-465_115-456dup
NM_000619.3:c.115-465_115-456dup MANE Select NP_000610.2:n.115-465_115-456dup
Search 100 bp 5'
Search 100 bp 3'