Canonical Allele Identifier: CA129183025

Gene: IRGM

Linked Data

• dbSNP Id: rs563509360
• gnomAD v2: 5-150240121-C-T
• gnomAD v3: 5-150860559-C-T
• gnomAD v4: 5-150860559-C-T
• MyVariant Identifiers: chr5:g.150240121C>T (hg19) ; chr5:g.150860559C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860559C>T , CM000667.2:g.150860559C>T	GRCh38
NC_000005.9:g.150240121C>T , CM000667.1:g.150240121C>T	GRCh37
NC_000005.8:g.150220314C>T	NCBI36
NG_027809.2:g.19037C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000520549.1:c.158+11905C>T
XM_011537641.1:c.531+11905C>T	XP_011535943.1:n.531+11905C>T
NM_001346557.1:c.531+11905C>T	NP_001333486.1:n.531+11905C>T
NM_001346557.2:c.531+11905C>T	NP_001333486.1:n.531+11905C>T
NR_170598.1:n.1646+11905C>T