Canonical Allele Identifier: CA2043750542
Gene: IFNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156425T= , CM000674.2:g.68156425T= GRCh38
NC_000012.11:g.68550205T= , CM000674.1:g.68550205T= GRCh37
NC_000012.10:g.66836472T= NCBI36
NG_015840.1:g.8317A=

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.367-938A= MANE Select ENSP00000229135.3:n.367-938A=
ENST00000229135.3:c.367-938A= ENSP00000229135.3:n.367-938A=
NM_000619.2:c.367-938A= NP_000610.2:n.367-938A=
NM_000619.3:c.367-938A= MANE Select NP_000610.2:n.367-938A=
Search 100 bp 5'
Search 100 bp 3'