Canonical Allele Identifier: CA2043754762
Gene: IFNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158743G= , CM000674.2:g.68158743G= GRCh38
NC_000012.11:g.68552523G= , CM000674.1:g.68552523G= GRCh37
NC_000012.10:g.66838790G= NCBI36
NG_015840.1:g.5999C=

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-484C= MANE Select ENSP00000229135.3:n.115-484C=
ENST00000229135.3:c.115-484C= ENSP00000229135.3:n.115-484C=
NM_000619.2:c.115-484C= NP_000610.2:n.115-484C=
NM_000619.3:c.115-484C= MANE Select NP_000610.2:n.115-484C=