Canonical Allele Identifier: CA361785058

Gene: IRGM

Linked Data

• dbSNP Id: rs1157782183
• gnomAD v2: 5-150227807-A-G
• gnomAD v4: 5-150848245-A-G
• MyVariant Identifiers: chr5:g.150227807A>G (hg19) ; chr5:g.150848245A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848245A>G , CM000667.2:g.150848245A>G	GRCh38
NC_000005.9:g.150227807A>G , CM000667.1:g.150227807A>G	GRCh37
NC_000005.8:g.150208000A>G	NCBI36
NG_027809.1:g.6723A>G
NG_027809.2:g.6723A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000522154.2:c.122A>G MANE Select	ENSP00000428220.1:p.Asp41Gly
ENST00000522154.1:c.122A>G	ENSP00000428220.1:p.Asp41Gly
NM_001145805.1:c.122A>G	NP_001139277.1:p.Asp41Gly
XM_011537641.1:c.122A>G	XP_011535943.1:p.Asp41Gly
NM_001346557.1:c.122A>G	NP_001333486.1:p.Asp41Gly
NM_001346557.2:c.122A>G	NP_001333486.1:p.Asp41Gly
NM_001145805.2:c.122A>G MANE Select	NP_001139277.1:p.Asp41Gly
NR_170598.1:n.1237A>G