Canonical Allele Identifier: CA12336131

Gene: IFNGR1

Linked Data

• dbSNP Id: rs1327474
• gnomAD v2: 6-137541075-C-T
• gnomAD v3: 6-137219938-C-T
• gnomAD v4: 6-137219938-C-T
• MyVariant Identifiers: chr6:g.137541075C>T (hg19) ; chr6:g.137219938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137219938C>T , CM000668.2:g.137219938C>T	GRCh38
NC_000006.11:g.137541075C>T , CM000668.1:g.137541075C>T	GRCh37
NC_000006.10:g.137582768C>T	NCBI36
NG_007394.1:g.4493G>A , LRG_66:g.4493G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011535793.2:c.-752G>A	XP_011534095.1:n.-752G>A