Canonical Allele Identifier: CA361785532
Gene: IRGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150848442G>C , CM000667.2:g.150848442G>C GRCh38
NC_000005.9:g.150228004G>C , CM000667.1:g.150228004G>C GRCh37
NC_000005.8:g.150208197G>C NCBI36
NG_027809.1:g.6920G>C
NG_027809.2:g.6920G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000522154.2:c.319G>C MANE Select ENSP00000428220.1:p.Glu107Gln
ENST00000522154.1:c.319G>C ENSP00000428220.1:p.Glu107Gln
NM_001145805.1:c.319G>C NP_001139277.1:p.Glu107Gln
XM_011537641.1:c.319G>C XP_011535943.1:p.Glu107Gln
NM_001346557.1:c.319G>C NP_001333486.1:p.Glu107Gln
NM_001346557.2:c.319G>C NP_001333486.1:p.Glu107Gln
NM_001145805.2:c.319G>C MANE Select NP_001139277.1:p.Glu107Gln
NR_170598.1:n.1434G>C