Canonical Allele Identifier: CA563587145
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1256758214

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150860614C>A , CM000667.2:g.150860614C>A GRCh38
NC_000005.9:g.150240176C>A , CM000667.1:g.150240176C>A GRCh37
NC_000005.8:g.150220369C>A NCBI36
NG_027809.2:g.19092C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000520549.1:c.158+11960C>A
XM_011537641.1:c.531+11960C>A XP_011535943.1:n.531+11960C>A
NM_001346557.1:c.531+11960C>A NP_001333486.1:n.531+11960C>A
NM_001346557.2:c.531+11960C>A NP_001333486.1:n.531+11960C>A
NR_170598.1:n.1646+11960C>A