Canonical Allele Identifier: CA129183028
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs4566778

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860568T>C , CM000667.2:g.150860568T>C GRCh38
NC_000005.9:g.150240130T>C , CM000667.1:g.150240130T>C GRCh37
NC_000005.8:g.150220323T>C NCBI36
NG_027809.2:g.19046T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11914T>C
XM_011537641.1:c.531+11914T>C XP_011535943.1:n.531+11914T>C
NM_001346557.1:c.531+11914T>C NP_001333486.1:n.531+11914T>C
NM_001346557.2:c.531+11914T>C NP_001333486.1:n.531+11914T>C
NR_170598.1:n.1646+11914T>C