Canonical Allele Identifier: CA2043750443
Gene: IFNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156365T= , CM000674.2:g.68156365T= GRCh38
NC_000012.11:g.68550145T= , CM000674.1:g.68550145T= GRCh37
NC_000012.10:g.66836412T= NCBI36
NG_015840.1:g.8377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.367-878A= MANE Select ENSP00000229135.3:n.367-878A=
ENST00000229135.3:c.367-878A= ENSP00000229135.3:n.367-878A=
NM_000619.2:c.367-878A= NP_000610.2:n.367-878A=
NM_000619.3:c.367-878A= MANE Select NP_000610.2:n.367-878A=
Search 100 bp 5'
Search 100 bp 3'