Canonical Allele Identifier: CA691232860
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1229664911

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158689T>C , CM000674.2:g.68158689T>C GRCh38
NC_000012.11:g.68552469T>C , CM000674.1:g.68552469T>C GRCh37
NC_000012.10:g.66838736T>C NCBI36
NG_015840.1:g.6053A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-430A>G MANE Select ENSP00000229135.3:n.115-430A>G
ENST00000229135.3:c.115-430A>G ENSP00000229135.3:n.115-430A>G
NM_000619.2:c.115-430A>G NP_000610.2:n.115-430A>G
NM_000619.3:c.115-430A>G MANE Select NP_000610.2:n.115-430A>G