Canonical Allele Identifier: CA1591137826
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754121923

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860585A>G , CM000667.2:g.150860585A>G GRCh38
NC_000005.9:g.150240147A>G , CM000667.1:g.150240147A>G GRCh37
NC_000005.8:g.150220340A>G NCBI36
NG_027809.2:g.19063A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11931A>G
XM_011537641.1:c.531+11931A>G XP_011535943.1:n.531+11931A>G
NM_001346557.1:c.531+11931A>G NP_001333486.1:n.531+11931A>G
NM_001346557.2:c.531+11931A>G NP_001333486.1:n.531+11931A>G
NR_170598.1:n.1646+11931A>G