Canonical Allele Identifier: CA238116427
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1030523432
gnomAD v2: 12-68550216-G-A
gnomAD v3: 12-68156436-G-A
gnomAD v4: 12-68156436-G-A
MyVariant Identifiers: chr12:g.68550216G>A (hg19) chr12:g.68156436G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156436G>A , CM000674.2:g.68156436G>A GRCh38
NC_000012.11:g.68550216G>A , CM000674.1:g.68550216G>A GRCh37
NC_000012.10:g.66836483G>A NCBI36
NG_015840.1:g.8306C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.367-949C>T MANE Select ENSP00000229135.3:n.367-949C>T
ENST00000229135.3:c.367-949C>T ENSP00000229135.3:n.367-949C>T
NM_000619.2:c.367-949C>T NP_000610.2:n.367-949C>T
NM_000619.3:c.367-949C>T MANE Select NP_000610.2:n.367-949C>T
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