Canonical Allele Identifier: CA129188509
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs11747270

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150879305A>G , CM000667.2:g.150879305A>G GRCh38
NC_000005.9:g.150258867A>G , CM000667.1:g.150258867A>G GRCh37
NC_000005.8:g.150239060A>G NCBI36
NG_027809.2:g.37783A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.294-280A>G
XM_011537641.1:c.532-280A>G XP_011535943.1:n.532-280A>G
NM_001346557.1:c.532-280A>G NP_001333486.1:n.532-280A>G
NM_001346557.2:c.532-280A>G NP_001333486.1:n.532-280A>G
NR_170598.1:n.1782-280A>G