Canonical Allele Identifier: CA805659595

Gene: IRGM

Linked Data

• dbSNP Id: rs1404837246
• MyVariant Identifiers: chr5:g.150239624_150239625insG (hg19) ; chr5:g.150860062_150860063insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860063dup , CM000667.2:g.150860063dup	GRCh38
NC_000005.9:g.150239625dup , CM000667.1:g.150239625dup	GRCh37
NC_000005.8:g.150219818dup	NCBI36
NG_027809.2:g.18541dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000520549.1:c.158+11409dup
XM_011537641.1:c.531+11409dup	XP_011535943.1:n.531+11409dup
NM_001346557.1:c.531+11409dup	NP_001333486.1:n.531+11409dup
NM_001346557.2:c.531+11409dup	NP_001333486.1:n.531+11409dup
NR_170598.1:n.1646+11409dup