Canonical Allele Identifier: CA691232851
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1219645996
gnomAD v3: 12-68158682-C-A
gnomAD v4: 12-68158682-C-A
MyVariant Identifiers: chr12:g.68552462C>A (hg19) chr12:g.68158682C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158682C>A , CM000674.2:g.68158682C>A GRCh38
NC_000012.11:g.68552462C>A , CM000674.1:g.68552462C>A GRCh37
NC_000012.10:g.66838729C>A NCBI36
NG_015840.1:g.6060G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-423G>T MANE Select ENSP00000229135.3:n.115-423G>T
ENST00000229135.3:c.115-423G>T ENSP00000229135.3:n.115-423G>T
NM_000619.2:c.115-423G>T NP_000610.2:n.115-423G>T
NM_000619.3:c.115-423G>T MANE Select NP_000610.2:n.115-423G>T
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