Canonical Allele Identifier: CA2043750643
Gene: IFNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156479G= , CM000674.2:g.68156479G= GRCh38
NC_000012.11:g.68550259G= , CM000674.1:g.68550259G= GRCh37
NC_000012.10:g.66836526G= NCBI36
NG_015840.1:g.8263C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.367-992C= MANE Select ENSP00000229135.3:n.367-992C=
ENST00000229135.3:c.367-992C= ENSP00000229135.3:n.367-992C=
NM_000619.2:c.367-992C= NP_000610.2:n.367-992C=
NM_000619.3:c.367-992C= MANE Select NP_000610.2:n.367-992C=
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