Canonical Allele Identifier: CA361785555
Gene: IRGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848448C>A , CM000667.2:g.150848448C>A GRCh38
NC_000005.9:g.150228010C>A , CM000667.1:g.150228010C>A GRCh37
NC_000005.8:g.150208203C>A NCBI36
NG_027809.1:g.6926C>A
NG_027809.2:g.6926C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.325C>A MANE Select ENSP00000428220.1:p.Gln109Lys
ENST00000522154.1:c.325C>A ENSP00000428220.1:p.Gln109Lys
NM_001145805.1:c.325C>A NP_001139277.1:p.Gln109Lys
XM_011537641.1:c.325C>A XP_011535943.1:p.Gln109Lys
NM_001346557.1:c.325C>A NP_001333486.1:p.Gln109Lys
NM_001346557.2:c.325C>A NP_001333486.1:p.Gln109Lys
NM_001145805.2:c.325C>A MANE Select NP_001139277.1:p.Gln109Lys
NR_170598.1:n.1440C>A