Canonical Allele Identifier: CA230528
Gene: IFNG HGNC NCBI

Linked Data

ClinVar Variation Id: 111224
ClinVar RCV Id: RCV000097426
dbSNP Id: rs121913164
gnomAD v2: 12-68551554-A-G
gnomAD v3: 12-68157774-A-G
gnomAD v4: 12-68157774-A-G
MyVariant Identifiers: chr12:g.68551554A>G (hg19) chr12:g.68157774A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68157774A>G , CM000674.2:g.68157774A>G GRCh38
NC_000012.11:g.68551554A>G , CM000674.1:g.68551554A>G GRCh37
NC_000012.10:g.66837821A>G NCBI36
NG_015840.1:g.6968T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.366+139T>C MANE Select ENSP00000229135.3:n.366+139T>C
ENST00000229135.3:c.366+139T>C ENSP00000229135.3:n.366+139T>C
NM_000619.2:c.366+139T>C NP_000610.2:n.366+139T>C
NM_000619.3:c.366+139T>C MANE Select NP_000610.2:n.366+139T>C
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