Canonical Allele Identifier: CA1591131982
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848254A= , CM000667.2:g.150848254A= GRCh38
NC_000005.9:g.150227816A= , CM000667.1:g.150227816A= GRCh37
NC_000005.8:g.150208009A= NCBI36
NG_027809.1:g.6732A=
NG_027809.2:g.6732A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000522154.2:c.131A= MANE Select ENSP00000428220.1:p.Asn44=
ENST00000522154.1:c.131A= ENSP00000428220.1:p.Asn44=
NM_001145805.1:c.131A= NP_001139277.1:p.Asn44=
XM_011537641.1:c.131A= XP_011535943.1:p.Asn44=
NM_001346557.1:c.131A= NP_001333486.1:p.Asn44=
NM_001346557.2:c.131A= NP_001333486.1:p.Asn44=
NM_001145805.2:c.131A= MANE Select NP_001139277.1:p.Asn44=
NR_170598.1:n.1246A=