Canonical Allele Identifier: CA948825872
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1882639602

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158675T>A , CM000674.2:g.68158675T>A GRCh38
NC_000012.11:g.68552455T>A , CM000674.1:g.68552455T>A GRCh37
NC_000012.10:g.66838722T>A NCBI36
NG_015840.1:g.6067A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-416A>T MANE Select ENSP00000229135.3:n.115-416A>T
ENST00000229135.3:c.115-416A>T ENSP00000229135.3:n.115-416A>T
NM_000619.2:c.115-416A>T NP_000610.2:n.115-416A>T
NM_000619.3:c.115-416A>T MANE Select NP_000610.2:n.115-416A>T