Canonical Allele Identifier: CA129176766

Gene: IRGM

Linked Data

• dbSNP Id: rs962229683
• MyVariant Identifiers: chr5:g.150227809T>G (hg19) ; chr5:g.150848247T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848247T>G , CM000667.2:g.150848247T>G	GRCh38
NC_000005.9:g.150227809T>G , CM000667.1:g.150227809T>G	GRCh37
NC_000005.8:g.150208002T>G	NCBI36
NG_027809.1:g.6725T>G
NG_027809.2:g.6725T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522154.2:c.124T>G MANE Select	ENSP00000428220.1:p.Ser42Ala
ENST00000522154.1:c.124T>G	ENSP00000428220.1:p.Ser42Ala
NM_001145805.1:c.124T>G	NP_001139277.1:p.Ser42Ala
XM_011537641.1:c.124T>G	XP_011535943.1:p.Ser42Ala
NM_001346557.1:c.124T>G	NP_001333486.1:p.Ser42Ala
NM_001346557.2:c.124T>G	NP_001333486.1:p.Ser42Ala
NM_001145805.2:c.124T>G MANE Select	NP_001139277.1:p.Ser42Ala
NR_170598.1:n.1239T>G