Canonical Allele Identifier: CA1591138021
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754128546

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861041G>C , CM000667.2:g.150861041G>C GRCh38
NC_000005.9:g.150240603G>C , CM000667.1:g.150240603G>C GRCh37
NC_000005.8:g.150220796G>C NCBI36
NG_027809.2:g.19519G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12387G>C
XM_011537641.1:c.531+12387G>C XP_011535943.1:n.531+12387G>C
NM_001346557.1:c.531+12387G>C NP_001333486.1:n.531+12387G>C
NM_001346557.2:c.531+12387G>C NP_001333486.1:n.531+12387G>C
NR_170598.1:n.1646+12387G>C