Canonical Allele Identifier: CA2726520783
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs2120741373
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68156338C>T , CM000674.2:g.68156338C>T GRCh38
NC_000012.11:g.68550118C>T , CM000674.1:g.68550118C>T GRCh37
NC_000012.10:g.66836385C>T NCBI36
NG_015840.1:g.8404G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229135.4:c.367-851G>A MANE Select ENSP00000229135.3:n.367-851G>A
ENST00000229135.3:c.367-851G>A ENSP00000229135.3:n.367-851G>A
NM_000619.2:c.367-851G>A NP_000610.2:n.367-851G>A
NM_000619.3:c.367-851G>A MANE Select NP_000610.2:n.367-851G>A
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