Canonical Allele Identifier: CA1591137822
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860579G= , CM000667.2:g.150860579G= GRCh38
NC_000005.9:g.150240141G= , CM000667.1:g.150240141G= GRCh37
NC_000005.8:g.150220334G= NCBI36
NG_027809.2:g.19057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11925G=
XM_011537641.1:c.531+11925G= XP_011535943.1:n.531+11925G=
NM_001346557.1:c.531+11925G= NP_001333486.1:n.531+11925G=
NM_001346557.2:c.531+11925G= NP_001333486.1:n.531+11925G=
NR_170598.1:n.1646+11925G=