Canonical Allele Identifier: CA805659745

Gene: IRGM

Linked Data

• dbSNP Id: rs1216555216
• MyVariant Identifiers: chr5:g.150239961_150239966del (hg19) ; chr5:g.150860399_150860404del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860402_150860407del , CM000667.2:g.150860402_150860407del	GRCh38
NC_000005.9:g.150239964_150239969del , CM000667.1:g.150239964_150239969del	GRCh37
NC_000005.8:g.150220157_150220162del	NCBI36
NG_027809.2:g.18880_18885del

Transcript Alleles

HGVS	Amino-acid change
ENST00000520549.1:c.158+11748_158+11753del
XM_011537641.1:c.531+11748_531+11753del	XP_011535943.1:n.531+11748_531+11753del
NM_001346557.1:c.531+11748_531+11753del	NP_001333486.1:n.531+11748_531+11753del
NM_001346557.2:c.531+11748_531+11753del	NP_001333486.1:n.531+11748_531+11753del
NR_170598.1:n.1646+11748_1646+11753del