Canonical Allele Identifier: CA1591137752
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860416C= , CM000667.2:g.150860416C= GRCh38
NC_000005.9:g.150239978C= , CM000667.1:g.150239978C= GRCh37
NC_000005.8:g.150220171C= NCBI36
NG_027809.2:g.18894C=

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11762C=
XM_011537641.1:c.531+11762C= XP_011535943.1:n.531+11762C=
NM_001346557.1:c.531+11762C= NP_001333486.1:n.531+11762C=
NM_001346557.2:c.531+11762C= NP_001333486.1:n.531+11762C=
NR_170598.1:n.1646+11762C=