Canonical Allele Identifier: CA1591137797
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860522T= , CM000667.2:g.150860522T= GRCh38
NC_000005.9:g.150240084T= , CM000667.1:g.150240084T= GRCh37
NC_000005.8:g.150220277T= NCBI36
NG_027809.2:g.19000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11868T=
XM_011537641.1:c.531+11868T= XP_011535943.1:n.531+11868T=
NM_001346557.1:c.531+11868T= NP_001333486.1:n.531+11868T=
NM_001346557.2:c.531+11868T= NP_001333486.1:n.531+11868T=
NR_170598.1:n.1646+11868T=