Canonical Allele Identifier: CA129183007
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1028517800

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860508T>G , CM000667.2:g.150860508T>G GRCh38
NC_000005.9:g.150240070T>G , CM000667.1:g.150240070T>G GRCh37
NC_000005.8:g.150220263T>G NCBI36
NG_027809.2:g.18986T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11854T>G
XM_011537641.1:c.531+11854T>G XP_011535943.1:n.531+11854T>G
NM_001346557.1:c.531+11854T>G NP_001333486.1:n.531+11854T>G
NM_001346557.2:c.531+11854T>G NP_001333486.1:n.531+11854T>G
NR_170598.1:n.1646+11854T>G