Canonical Allele Identifier: CA563587152

Gene: IRGM

Linked Data

• dbSNP Id: rs1165926752
• gnomAD v2: 5-150240276-TCTGCTG-T
• gnomAD v3: 5-150860714-TCTGCTG-T
• gnomAD v4: 5-150860714-TCTGCTG-T
• MyVariant Identifiers: chr5:g.150240277_150240282del (hg19) ; chr5:g.150860715_150860720del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860719_150860724del , CM000667.2:g.150860719_150860724del	GRCh38
NC_000005.9:g.150240281_150240286del , CM000667.1:g.150240281_150240286del	GRCh37
NC_000005.8:g.150220474_150220479del	NCBI36
NG_027809.2:g.19197_19202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520549.1:c.158+12065_158+12070del
XM_011537641.1:c.531+12065_531+12070del	XP_011535943.1:n.531+12065_531+12070del
NM_001346557.1:c.531+12065_531+12070del	NP_001333486.1:n.531+12065_531+12070del
NM_001346557.2:c.531+12065_531+12070del	NP_001333486.1:n.531+12065_531+12070del
NR_170598.1:n.1646+12065_1646+12070del