Canonical Allele Identifier: CA691232864
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1431148714
gnomAD v3: 12-68158700-TCC-T
gnomAD v4: 12-68158700-TCC-T
MyVariant Identifiers: chr12:g.68552481_68552482del (hg19) chr12:g.68158701_68158702del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158701_68158702del , CM000674.2:g.68158701_68158702del GRCh38
NC_000012.11:g.68552481_68552482del , CM000674.1:g.68552481_68552482del GRCh37
NC_000012.10:g.66838748_66838749del NCBI36
NG_015840.1:g.6040_6041del

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.115-443_115-442del MANE Select ENSP00000229135.3:n.115-443_115-442del
ENST00000229135.3:c.115-443_115-442del ENSP00000229135.3:n.115-443_115-442del
NM_000619.2:c.115-443_115-442del NP_000610.2:n.115-443_115-442del
NM_000619.3:c.115-443_115-442del MANE Select NP_000610.2:n.115-443_115-442del
Search 100 bp 5'
Search 100 bp 3'