Canonical Allele Identifier: CA361785086

Gene: IRGM

Linked Data

• gnomAD v4: 5-150848257-G-T
• MyVariant Identifiers: chr5:g.150227819G>T (hg19) ; chr5:g.150848257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150848257G>T , CM000667.2:g.150848257G>T	GRCh38
NC_000005.9:g.150227819G>T , CM000667.1:g.150227819G>T	GRCh37
NC_000005.8:g.150208012G>T	NCBI36
NG_027809.1:g.6735G>T
NG_027809.2:g.6735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522154.2:c.134G>T MANE Select	ENSP00000428220.1:p.Gly45Val
ENST00000522154.1:c.134G>T	ENSP00000428220.1:p.Gly45Val
NM_001145805.1:c.134G>T	NP_001139277.1:p.Gly45Val
XM_011537641.1:c.134G>T	XP_011535943.1:p.Gly45Val
NM_001346557.1:c.134G>T	NP_001333486.1:p.Gly45Val
NM_001346557.2:c.134G>T	NP_001333486.1:p.Gly45Val
NM_001145805.2:c.134G>T MANE Select	NP_001139277.1:p.Gly45Val
NR_170598.1:n.1249G>T