Canonical Allele Identifier: CA691232866
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1342320288
gnomAD v3: 12-68158701-C-G
gnomAD v4: 12-68158701-C-G
MyVariant Identifiers: chr12:g.68552481C>G (hg19) chr12:g.68158701C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158701C>G , CM000674.2:g.68158701C>G GRCh38
NC_000012.11:g.68552481C>G , CM000674.1:g.68552481C>G GRCh37
NC_000012.10:g.66838748C>G NCBI36
NG_015840.1:g.6041G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-442G>C MANE Select ENSP00000229135.3:n.115-442G>C
ENST00000229135.3:c.115-442G>C ENSP00000229135.3:n.115-442G>C
NM_000619.2:c.115-442G>C NP_000610.2:n.115-442G>C
NM_000619.3:c.115-442G>C MANE Select NP_000610.2:n.115-442G>C
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