Canonical Allele Identifier: CA2043754460
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1565726228

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158677T>C , CM000674.2:g.68158677T>C GRCh38
NC_000012.11:g.68552457T>C , CM000674.1:g.68552457T>C GRCh37
NC_000012.10:g.66838724T>C NCBI36
NG_015840.1:g.6065A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-418A>G MANE Select ENSP00000229135.3:n.115-418A>G
ENST00000229135.3:c.115-418A>G ENSP00000229135.3:n.115-418A>G
NM_000619.2:c.115-418A>G NP_000610.2:n.115-418A>G
NM_000619.3:c.115-418A>G MANE Select NP_000610.2:n.115-418A>G