Canonical Allele Identifier: CA1591137577
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754113002

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150859977C>T , CM000667.2:g.150859977C>T GRCh38
NC_000005.9:g.150239539C>T , CM000667.1:g.150239539C>T GRCh37
NC_000005.8:g.150219732C>T NCBI36
NG_027809.2:g.18455C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+11323C>T
XM_011537641.1:c.531+11323C>T XP_011535943.1:n.531+11323C>T
NM_001346557.1:c.531+11323C>T NP_001333486.1:n.531+11323C>T
NM_001346557.2:c.531+11323C>T NP_001333486.1:n.531+11323C>T
NR_170598.1:n.1646+11323C>T