Canonical Allele Identifier: CA948825079
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs1882600582
gnomAD v3: 12-68156314-G-A
gnomAD v4: 12-68156314-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156314G>A , CM000674.2:g.68156314G>A GRCh38
NC_000012.11:g.68550094G>A , CM000674.1:g.68550094G>A GRCh37
NC_000012.10:g.66836361G>A NCBI36
NG_015840.1:g.8428C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.367-827C>T MANE Select ENSP00000229135.3:n.367-827C>T
ENST00000229135.3:c.367-827C>T ENSP00000229135.3:n.367-827C>T
NM_000619.2:c.367-827C>T NP_000610.2:n.367-827C>T
NM_000619.3:c.367-827C>T MANE Select NP_000610.2:n.367-827C>T
Search 100 bp 5'
Search 100 bp 3'