Canonical Allele Identifier: CA948825461
Gene: IFNG HGNC NCBI
gnomAD v3:
12:68157416 G / T
gnomAD v4:
chr12-68157416-G-T
Joint Max Group AF 0.00005293 (AMR)
Genomes Max Group AF 0.00005293 (AMR)
dbSNP:
1861493
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68157416G>T , CM000674.2:g.68157416G>T GRCh38
NC_000012.11:g.68551196G>T , CM000674.1:g.68551196G>T GRCh37
NC_000012.10:g.66837463G>T NCBI36
NG_015840.1:g.7326C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.366+497C>A MANE Select ENSP00000229135.3:n.366+497C>A
ENST00000229135.3:c.366+497C>A ENSP00000229135.3:n.366+497C>A
NM_000619.2:c.366+497C>A NP_000610.2:n.366+497C>A
NM_000619.3:c.366+497C>A MANE Select NP_000610.2:n.366+497C>A
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