Canonical Allele Identifier: CA129183016
Gene: IRGM HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1000113

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860514C>T , CM000667.2:g.150860514C>T GRCh38
NC_000005.9:g.150240076C>T , CM000667.1:g.150240076C>T GRCh37
NC_000005.8:g.150220269C>T NCBI36
NG_027809.2:g.18992C>T

Transcript Alleles

HGVS Amino-acid change
XM_011537641.1:c.531+11860C>T XP_011535943.1:p.=
NM_001346557.1:c.531+11860C>T VV NP_001333486.1:p.=
ENST00000520549.1:n.158+11860C>T