Canonical Allele Identifier: CA2043754398
Gene: IFNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158665T= , CM000674.2:g.68158665T= GRCh38
NC_000012.11:g.68552445T= , CM000674.1:g.68552445T= GRCh37
NC_000012.10:g.66838712T= NCBI36
NG_015840.1:g.6077A=

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-406A= MANE Select ENSP00000229135.3:n.115-406A=
ENST00000229135.3:c.115-406A= ENSP00000229135.3:n.115-406A=
NM_000619.2:c.115-406A= NP_000610.2:n.115-406A=
NM_000619.3:c.115-406A= MANE Select NP_000610.2:n.115-406A=