Canonical Allele Identifier: CA2043754473
Gene: IFNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158681A= , CM000674.2:g.68158681A= GRCh38
NC_000012.11:g.68552461A= , CM000674.1:g.68552461A= GRCh37
NC_000012.10:g.66838728A= NCBI36
NG_015840.1:g.6061T=

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-422T= MANE Select ENSP00000229135.3:n.115-422T=
ENST00000229135.3:c.115-422T= ENSP00000229135.3:n.115-422T=
NM_000619.2:c.115-422T= NP_000610.2:n.115-422T=
NM_000619.3:c.115-422T= MANE Select NP_000610.2:n.115-422T=