Canonical Allele Identifier: CA1591138028
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861053T= , CM000667.2:g.150861053T= GRCh38
NC_000005.9:g.150240615T= , CM000667.1:g.150240615T= GRCh37
NC_000005.8:g.150220808T= NCBI36
NG_027809.2:g.19531T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12399T=
XM_011537641.1:c.531+12399T= XP_011535943.1:n.531+12399T=
NM_001346557.1:c.531+12399T= NP_001333486.1:n.531+12399T=
NM_001346557.2:c.531+12399T= NP_001333486.1:n.531+12399T=
NR_170598.1:n.1646+12399T=