Canonical Allele Identifier: CA129182885

Gene: IRGM

Linked Data

• dbSNP Id: rs982261535
• gnomAD v3: 5-150860311-T-A
• gnomAD v4: 5-150860311-T-A
• MyVariant Identifiers: chr5:g.150239873T>A (hg19) ; chr5:g.150860311T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860311T>A , CM000667.2:g.150860311T>A	GRCh38
NC_000005.9:g.150239873T>A , CM000667.1:g.150239873T>A	GRCh37
NC_000005.8:g.150220066T>A	NCBI36
NG_027809.2:g.18789T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000520549.1:c.158+11657T>A
XM_011537641.1:c.531+11657T>A	XP_011535943.1:n.531+11657T>A
NM_001346557.1:c.531+11657T>A	NP_001333486.1:n.531+11657T>A
NM_001346557.2:c.531+11657T>A	NP_001333486.1:n.531+11657T>A
NR_170598.1:n.1646+11657T>A