Canonical Allele Identifier: CA563587184

Gene: IRGM

Linked Data

• dbSNP Id: rs1380710756
• gnomAD v2: 5-150240522-C-G
• gnomAD v3: 5-150860960-C-G
• gnomAD v4: 5-150860960-C-G
• MyVariant Identifiers: chr5:g.150240522C>G (hg19) ; chr5:g.150860960C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150860960C>G , CM000667.2:g.150860960C>G	GRCh38
NC_000005.9:g.150240522C>G , CM000667.1:g.150240522C>G	GRCh37
NC_000005.8:g.150220715C>G	NCBI36
NG_027809.2:g.19438C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000520549.1:c.158+12306C>G
XM_011537641.1:c.531+12306C>G	XP_011535943.1:n.531+12306C>G
NM_001346557.1:c.531+12306C>G	NP_001333486.1:n.531+12306C>G
NM_001346557.2:c.531+12306C>G	NP_001333486.1:n.531+12306C>G
NR_170598.1:n.1646+12306C>G