Canonical Allele Identifier: CA13669591

Gene: IFNG

Linked Data

• dbSNP Id: rs2430561
• gnomAD v2: 12-68552522-T-A
• gnomAD v3: 12-68158742-T-A
• gnomAD v4: 12-68158742-T-A
• MyVariant Identifiers: chr12:g.68552522T>A (hg19) ; chr12:g.68158742T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68158742T>A , CM000674.2:g.68158742T>A	GRCh38
NC_000012.11:g.68552522T>A , CM000674.1:g.68552522T>A	GRCh37
NC_000012.10:g.66838789T>A	NCBI36
NG_015840.1:g.6000A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229135.4:c.115-483A>T MANE Select	ENSP00000229135.3:n.115-483A>T
ENST00000229135.3:c.115-483A>T	ENSP00000229135.3:n.115-483A>T
NM_000619.2:c.115-483A>T	NP_000610.2:n.115-483A>T
NM_000619.3:c.115-483A>T MANE Select	NP_000610.2:n.115-483A>T