Canonical Allele Identifier: CA129183016
Gene: IRGM HGNC NCBI

Linked Data

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
ENST00000520549.1:n.158+11860C>T
XM_011537641.1:c.531+11860C>T XP_011535943.1:n.531+11860C>T
NM_001346557.1:c.531+11860C>T NP_001333486.1:n.531+11860C>T
NM_001346557.2:c.531+11860C>T NP_001333486.1:n.531+11860C>T
NR_170598.1:n.1646+11860C>T