Canonical Allele Identifier: CA1591131983
Gene: IRGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848255T= , CM000667.2:g.150848255T= GRCh38
NC_000005.9:g.150227817T= , CM000667.1:g.150227817T= GRCh37
NC_000005.8:g.150208010T= NCBI36
NG_027809.1:g.6733T=
NG_027809.2:g.6733T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000522154.2:c.132T= MANE Select ENSP00000428220.1:p.Asn44=
ENST00000522154.1:c.132T= ENSP00000428220.1:p.Asn44=
NM_001145805.1:c.132T= NP_001139277.1:p.Asn44=
XM_011537641.1:c.132T= XP_011535943.1:p.Asn44=
NM_001346557.1:c.132T= NP_001333486.1:p.Asn44=
NM_001346557.2:c.132T= NP_001333486.1:p.Asn44=
NM_001145805.2:c.132T= MANE Select NP_001139277.1:p.Asn44=
NR_170598.1:n.1247T=