Canonical Allele Identifier: CA1591138024
Gene: IRGM HGNC NCBI

Linked Data

dbSNP Id: rs1754128763

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150861049T>C , CM000667.2:g.150861049T>C GRCh38
NC_000005.9:g.150240611T>C , CM000667.1:g.150240611T>C GRCh37
NC_000005.8:g.150220804T>C NCBI36
NG_027809.2:g.19527T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000520549.1:c.158+12395T>C
XM_011537641.1:c.531+12395T>C XP_011535943.1:n.531+12395T>C
NM_001346557.1:c.531+12395T>C NP_001333486.1:n.531+12395T>C
NM_001346557.2:c.531+12395T>C NP_001333486.1:n.531+12395T>C
NR_170598.1:n.1646+12395T>C