Canonical Allele Identifier: CA6675902
Gene: IFNG HGNC NCBI

Linked Data

ClinVar Variation Id: 402962
ClinVar RCV Id: RCV000455108 RCV001683492 RCV001703173
dbSNP Id: rs2234686
ExAC: 12:68552041 TA / T
gnomAD v2: 12-68552041-TA-T
gnomAD v3: 12-68158261-TA-T
gnomAD v4: 12-68158261-TA-T
MyVariant Identifiers: chr12:g.68552045del (hg19) chr12:g.68552044del (hg19) chr12:g.68552042del (hg19) chr12:g.68158264del (hg38) chr12:g.68158262del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158274del , CM000674.2:g.68158274del GRCh38
NC_000012.11:g.68552054del , CM000674.1:g.68552054del GRCh37
NC_000012.10:g.66838321del NCBI36
NG_015840.1:g.6480del

Transcript Alleles

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