Canonical Allele Identifier: CA447412302

Gene: IRGM

Linked Data

• MyVariant Identifiers: chr5:g.150227901C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848339C>G , CM000667.2:g.150848339C>G	GRCh38
NC_000005.9:g.150227901C>G , CM000667.1:g.150227901C>G	GRCh37
NC_000005.8:g.150208094C>G	NCBI36
NG_027809.1:g.6817C>G
NG_027809.2:g.6817C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000522154.2:c.216C>G MANE Select	ENSP00000428220.1:p.Thr72=
ENST00000522154.1:c.216C>G	ENSP00000428220.1:p.Thr72=
NM_001145805.1:c.216C>G	NP_001139277.1:p.Thr72=
XM_011537641.1:c.216C>G	XP_011535943.1:p.Thr72=
NM_001346557.1:c.216C>G	NP_001333486.1:p.Thr72=
NM_001346557.2:c.216C>G	NP_001333486.1:p.Thr72=
NM_001145805.2:c.216C>G MANE Select	NP_001139277.1:p.Thr72=
NR_170598.1:n.1331C>G