Canonical Allele Identifier: CA805659697
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1443261152

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860325del , CM000667.2:g.150860325del GRCh38
NC_000005.9:g.150239887del , CM000667.1:g.150239887del GRCh37
NC_000005.8:g.150220080del NCBI36
NG_027809.2:g.18803del

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11671del
XM_011537641.1:c.531+11671del XP_011535943.1:n.531+11671del
NM_001346557.1:c.531+11671del NP_001333486.1:n.531+11671del
NM_001346557.2:c.531+11671del NP_001333486.1:n.531+11671del
NR_170598.1:n.1646+11671del