Canonical Allele Identifier: CA1591137799
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860523T= , CM000667.2:g.150860523T= GRCh38
NC_000005.9:g.150240085T= , CM000667.1:g.150240085T= GRCh37
NC_000005.8:g.150220278T= NCBI36
NG_027809.2:g.19001T=

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11869T=
XM_011537641.1:c.531+11869T= XP_011535943.1:n.531+11869T=
NM_001346557.1:c.531+11869T= NP_001333486.1:n.531+11869T=
NM_001346557.2:c.531+11869T= NP_001333486.1:n.531+11869T=
NR_170598.1:n.1646+11869T=