Canonical Allele Identifier: CA805659979

Gene: IRGM

Linked Data

• dbSNP Id: rs1237744732
• gnomAD v3: 5-150860723-GCCTTGGGA-G
• gnomAD v4: 5-150860723-GCCTTGGGA-G
• MyVariant Identifiers: chr5:g.150240286_150240293del (hg19) ; chr5:g.150860724_150860731del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860727_150860734del , CM000667.2:g.150860727_150860734del	GRCh38
NC_000005.9:g.150240289_150240296del , CM000667.1:g.150240289_150240296del	GRCh37
NC_000005.8:g.150220482_150220489del	NCBI36
NG_027809.2:g.19205_19212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520549.1:c.158+12073_158+12080del
XM_011537641.1:c.531+12073_531+12080del	XP_011535943.1:n.531+12073_531+12080del
NM_001346557.1:c.531+12073_531+12080del	NP_001333486.1:n.531+12073_531+12080del
NM_001346557.2:c.531+12073_531+12080del	NP_001333486.1:n.531+12073_531+12080del
NR_170598.1:n.1646+12073_1646+12080del