Canonical Allele Identifier: CA129183267
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs184266220
MyVariant Identifiers: chr5:g.150240578C>A (hg19) chr5:g.150861016C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861016C>A , CM000667.2:g.150861016C>A GRCh38
NC_000005.9:g.150240578C>A , CM000667.1:g.150240578C>A GRCh37
NC_000005.8:g.150220771C>A NCBI36
NG_027809.2:g.19494C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12362C>A
XM_011537641.1:c.531+12362C>A XP_011535943.1:n.531+12362C>A
NM_001346557.1:c.531+12362C>A NP_001333486.1:n.531+12362C>A
NM_001346557.2:c.531+12362C>A NP_001333486.1:n.531+12362C>A
NR_170598.1:n.1646+12362C>A
Search 100 bp 5'
Search 100 bp 3'