Canonical Allele Identifier: CA2043754393
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1882639206

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158653A>G , CM000674.2:g.68158653A>G GRCh38
NC_000012.11:g.68552433A>G , CM000674.1:g.68552433A>G GRCh37
NC_000012.10:g.66838700A>G NCBI36
NG_015840.1:g.6089T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-394T>C MANE Select ENSP00000229135.3:n.115-394T>C
ENST00000229135.3:c.115-394T>C ENSP00000229135.3:n.115-394T>C
NM_000619.2:c.115-394T>C NP_000610.2:n.115-394T>C
NM_000619.3:c.115-394T>C MANE Select NP_000610.2:n.115-394T>C